Canonical Allele Identifier: PA2826317882
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 2682332
ClinVar RCV Id: RCV003479705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ala750Thr
CA388015392
NM_001243182.2:c.2248G>A