Allele Registry

Canonical Allele Identifier: PA658674184

Gene: COMP HGNC NCBI

ClinVar Allele:

446075

ClinVar RCV:

RCV000521517

ClinVar Variation:

449474

HGVS (amino-acid)	Matching Registered Transcripts
NP_000086.2:p.Asp399Asn	CA404886685 NM_000095.3:c.1195G>A