Canonical Allele Identifier: PA2826317879
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1501800
ClinVar RCV Id: RCV002019924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr747Ala
CA388015660
NM_001243182.2:c.2239A>G