Canonical Allele Identifier: PA100751
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 40990
ClinVar RCV Id: RCV000033882 RCV000489545
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Thr529Ile
CA343855
NM_000095.3:c.1586C>T