Allele Registry

Canonical Allele Identifier: PA2825835877

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV002322688

ClinVar Variation:

1728485

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135445.1:p.Leu1054Arg	CA18625694 NM_001141973.3:c.3161T>G