Canonical Allele Identifier: PA2827326036
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1525062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317507.1:p.Gly791Glu
CA6988947
NM_001330578.2:c.2372G>A