Canonical Allele Identifier: PA2499228435
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1224328
ClinVar RCV Id: RCV001596866
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Gln492Pro
CA404884162
NM_000095.3:c.1475A>C