Canonical Allele Identifier: PA2826317923
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 100803
ClinVar RCV Id: RCV000087161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly780Ala
CA228984
NM_001243182.2:c.2339G>C