Canonical Allele Identifier: PA2826317995
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 189058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly832Asp
CA274329
NM_001243182.2:c.2495G>A