Allele Registry

Canonical Allele Identifier: PA2826318580

Gene: ATP7B HGNC NCBI

ClinVar Allele:

167803

ClinVar RCV:

RCV000145281

RCV003895025

ClinVar Variation:

157956

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Gly1236Ser	CA271178 NM_001243182.2:c.3706G>A