Allele Registry

Canonical Allele Identifier: PA2826317584

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000631234

ClinVar Variation:

526655

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Asp531Tyr	CA388027513 NM_001243182.2:c.1591G>T