Canonical Allele Identifier: PA2827329289
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1930912
ClinVar RCV Id: RCV002631301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317508.1:p.Thr810Ala
CA388034344
NM_001330579.2:c.2428A>G