clinvar.record:
    alias: 
    description: ClinVar archives reports of relationships among medically important variants and phenotypes. It records human variation, interpretations of the relationship specific variations to human health, and supporting evidence for each interpretation. Each ClinVar record (RCV identifier) represents an aggregated view of interpretations of  the same variation and condition from one or more submitters. Submissions for individual variation/phenotype combinations (SCV identifier) are also collected and made available separately. This collection references the Record Report, based on RCV accession.
    forward: http://www.ncbi.nlm.nih.gov/clinvar/${ac}/
    institution: National Center for Biotechnology Information (NCBI), NIH, Maryland
    location: USA
    more: http://www.ncbi.nlm.nih.gov/clinvar/
    name: ClinVar Record at NCBI
    pattern: ^RCV\d+(\.\d+)?$
    prefixed: false
    primary: false
    probe: http://www.ncbi.nlm.nih.gov/clinvar/RCV000033555.3/
    provider: ncbi
    provider_id: MIR:00100710
    redirect: http://www.ncbi.nlm.nih.gov/clinvar/$id/
    sort_score: 5
    state: 100:Up
    subject: gene; human; phenotype
    synonym: PSI-PAR
    test: RCV000033555.3
    type: scheme

ncbi/clinvar.record:
    for: clinvar.record
    type: synonym