Allele Registry

Canonical Allele Identifier: PA2826318326

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001852911

ClinVar Variation:

50883

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Gly1065Arg	CA351338 NM_001243182.2:c.3193G>A CA388026079 NM_001243182.2:c.3193G>C