Allele Registry

Canonical Allele Identifier: PA2826317662

Gene: ATP7B HGNC NCBI

ClinVar Allele:

166061

ClinVar RCV:

RCV000144365

RCV000497757

ClinVar Variation:

156281

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Gly599Ser	CA270731 NM_001243182.2:c.1795G>A