Canonical Allele Identifier: PA2826317900
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Ala763Val
CA252892
NM_001243182.2:c.2288C>T