Canonical Allele Identifier: PA100707
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 40997
ClinVar RCV Id: RCV000033889 RCV001390635
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Gly719Ser
CA343864
NM_000095.3:c.2155G>A