Canonical Allele Identifier: PA2827329219
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1525062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly785Glu
CA6988947
NM_001330579.2:c.2354G>A