Allele Registry

Canonical Allele Identifier: PA2826317755

Gene: ATP7B HGNC NCBI

ClinVar RCV:

RCV001985854

ClinVar Variation:

1480099

HGVS (amino-acid)	Matching Registered Transcripts
NP_001230111.1:p.Pro657Arg	CA388021777 NM_001243182.2:c.1970C>G