Allele Registry

Canonical Allele Identifier: PA2573281566

Gene: ATP13A2 HGNC NCBI

ClinVar Allele:

1419617

ClinVar RCV:

RCV001951745

ClinVar Variation:

1460808

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Val620Ala	CA338246505 NM_022089.4:c.1859T>C