Canonical Allele Identifier: PA2826317627
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 1948955
ClinVar RCV Id: RCV002685876

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gln569Arg
CA388025243
NM_001243182.2:c.1706A>G