Allele Registry

Canonical Allele Identifier: PA2826317748

Gene: ATP7B HGNC NCBI

ClinVar Allele:

18900

ClinVar RCV:

RCV000004065

ClinVar Variation:

3861

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Thr655Arg	CA252898 NM_001243182.2:c.1964C>G