Canonical Allele Identifier: PA2826317918
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 882966
ClinVar RCV Id: RCV001113063

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.His778Arg
CA388034442
NM_001243182.2:c.2333A>G