Canonical Allele Identifier: PA2827330169
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Gly1182Arg
CA252890
NM_001330579.2:c.3544G>A
CA388022028
NM_001330579.2:c.3544G>C