Allele Registry

Canonical Allele Identifier: PA2825836860

Gene: ATP13A2 HGNC NCBI

ClinVar Allele:

1022752

ClinVar RCV:

RCV001350763

ClinVar Variation:

1046235

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135446.1:p.Val648Ile	CA637026 NM_001141974.3:c.1942G>A