Canonical Allele Identifier: PA202979
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 197627
ClinVar RCV Id: RCV000178711 RCV000259246 RCV000354091 RCV000881662 RCV002485172 RCV002277410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Ala171Thr
CA202978
NM_000095.3:c.511G>A