Canonical Allele Identifier: PA2825279918
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1018093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Cys872Arg
CA388029778
NM_001005918.3:c.2614T>C