Canonical Allele Identifier: PA2826317901
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 157940
ClinVar RCV Id: RCV000145264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly764Arg
CA171302
NM_001243182.2:c.2290G>A
CA388034772
NM_001243182.2:c.2290G>C