Canonical Allele Identifier: PA2825279932
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 554311
ClinVar RCV Id: RCV000669922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Gly882Glu
CA388028869
NM_001005918.3:c.2645G>A