Allele Registry

Canonical Allele Identifier: PA916006171

Gene: ATP7B HGNC NCBI

ClinVar Allele:

186885

ClinVar RCV:

RCV000169142

ClinVar Variation:

188808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Gly990Arg	CA273987 NM_001243182.2:c.2968G>A CA388028531 NM_001243182.2:c.2968G>C