Allele Registry

Canonical Allele Identifier: PA2826317743

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000589178

ClinVar Variation:

495406

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Asp654Gly	CA388021872 NM_001243182.2:c.1961A>G