Canonical Allele Identifier: PA2826317929
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 811797

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr783Ile
CA388034326
NM_001243182.2:c.2348C>T