Canonical Allele Identifier: PA2825279707
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1930912
ClinVar RCV Id: RCV002631301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005918.1:p.Thr732Ala
CA388034344
NM_001005918.3:c.2194A>G