Canonical Allele Identifier: PA2825279671
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1525062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly707Glu
CA6988947
NM_001005918.3:c.2120G>A