Allele Registry

Canonical Allele Identifier: PA645471477

Gene: COMP HGNC NCBI

ClinVar RCV:

RCV000312363

RCV000394504

RCV001850749

RCV002521198

ClinVar Variation:

328611

HGVS (amino-acid)	Matching Registered Transcripts
NP_000086.2:p.Thr660Arg	CA9316214 NM_000095.3:c.1979C>G