Canonical Allele Identifier: PA915956815
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 803547
ClinVar RCV Id: RCV000990188
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp518His
CA404883300
NM_000095.3:c.1552G>C