Canonical Allele Identifier: PA2741808918
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2696896
ClinVar RCV Id: RCV003543695
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp357Phe
CA2697556420
NM_000095.3:c.1069_1070delinsTT