Allele Registry

Canonical Allele Identifier: PA100241

Gene: COMP HGNC NCBI

ClinVar RCV:

RCV000009768

ClinVar Variation:

9190

HGVS (amino-acid)	Matching Registered Transcripts
NP_000086.2:p.Asn453Ser	CA120168 NM_000095.3:c.1358A>G