Canonical Allele Identifier: PA2573061254
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1327423
ClinVar RCV Id: RCV001787703 RCV002236174 RCV003546716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Gly501Ser
CA404883789
NM_000095.3:c.1501G>A