Canonical Allele Identifier: PA343863
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 40996
ClinVar RCV Id: RCV000033888 RCV000254993
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.His587Arg
CA343862
NM_000095.3:c.1760A>G