Canonical Allele Identifier: PA2826318193
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 495411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly961Asp
CA388029839
NM_001243182.2:c.2882G>A