Canonical Allele Identifier: PA2826317641
Gene: ATP7B HGNC NCBI

Linked Data

ClinVar Variation Id: 3866
ClinVar RCV Id: RCV000004070
ClinVar Variation Id: 2180424
ClinVar RCV Id: RCV002619246
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230111.1:p.Gly580Arg
CA252903
NM_001243182.2:c.1738G>A
CA388024710
NM_001243182.2:c.1738G>C