Allele Registry

Canonical Allele Identifier: PA100766

Gene: COMP HGNC NCBI

ClinVar RCV:

RCV000033887

RCV001388112

RCV002054553

ClinVar Variation:

40995

HGVS (amino-acid)	Matching Registered Transcripts
NP_000086.2:p.Thr585Met	CA343861 NM_000095.3:c.1754C>T