Allele Registry

Canonical Allele Identifier: PA2826317773

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001527078

ClinVar Variation:

1172922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Trp668Cys	CA388020479 NM_001243182.2:c.2004G>T CA388020480 NM_001243182.2:c.2004G>C