clinvar:
    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 Variant identifier.
    forward: https://www.ncbi.nlm.nih.gov/clinvar/variation/${ac}
    institution: National Center for Biotechnology Information (NCBI), NIH, Maryland
    location: USA
    more: http://www.ncbi.nlm.nih.gov/clinvar/
    name: ClinVar Variant at NCBI
    pattern: ^\d+$
    prefixed: false
    primary: false
    probe: https://www.ncbi.nlm.nih.gov/clinvar/variation/12345
    provider: ncbi
    provider_id: MIR:00100796
    redirect: https://www.ncbi.nlm.nih.gov/clinvar/variation/$id
    sort_score: 5
    state: 99:Up
    subject: 
    synonym: Global Research Identifier Database
    test: 12345
    type: scheme

ncbi/clinvar:
    for: clinvar
    type: synonym