Allele Registry

Canonical Allele Identifier: PA109907

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV002322688

ClinVar Variation:

1728485

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Leu1059Arg	CA18625694 NM_022089.4:c.3176T>G