Allele Registry

Canonical Allele Identifier: PA100695

Gene: COMP HGNC NCBI

ClinVar RCV:

RCV000009772

RCV000033890

RCV002223755

RCV003989283

ClinVar Variation:

9194

HGVS (amino-acid)	Matching Registered Transcripts
NP_000086.2:p.Gly719Asp	CA120170 NM_000095.3:c.2156G>A