Canonical Allele Identifier: PA2826317930
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1930912
ClinVar RCV Id: RCV002631301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Thr783Ala
CA388034344
NM_001243182.2:c.2347A>G