Canonical Allele Identifier: PA2825066576
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 3069180
ClinVar RCV Id: RCV004006237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Glu618Asp
CA404878080
NM_000095.3:c.1854G>T
CA404878083
NM_000095.3:c.1854G>C