Canonical Allele Identifier: PA915956780
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 692028
ClinVar RCV Id: RCV000853301
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp439Asn
CA404885325
NM_000095.3:c.1315G>A