Canonical Allele Identifier: PA915956892
Gene: CP HGNC NCBI

Linked Data

ClinVar Variation Id: 498766
ClinVar RCV Id: RCV000592806 RCV001860175
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000087.2:p.Tyr239Phe
CA2661256
NM_000096.4:c.716A>T