Allele Registry

Canonical Allele Identifier: PA2826318205

Gene: ATP7B HGNC NCBI

ClinVar Allele:

411516

ClinVar RCV:

RCV000487452

ClinVar Variation:

424618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Cys968Phe	CA16621524 NM_001243182.2:c.2903G>T