Canonical Allele Identifier: PA2826317564
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly515Ala
CA271167
NM_001243182.2:c.1544G>C