Canonical Allele Identifier: PA645510102
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 438839
ClinVar RCV Id: RCV000505823
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp376Tyr
CA404887723
NM_000095.3:c.1126G>T