Allele Registry

Canonical Allele Identifier: PA2825836813

Gene: ATP13A2 HGNC NCBI

ClinVar Allele:

1419617

ClinVar RCV:

RCV001951745

ClinVar Variation:

1460808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135446.1:p.Val615Ala	CA338246505 NM_001141974.3:c.1844T>C