Allele Registry

Canonical Allele Identifier: PA2826317996

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV000674965

ClinVar Variation:

558661

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Gly832Cys	CA388033415 NM_001243182.2:c.2494G>T