Allele Registry

Canonical Allele Identifier: PA2825835870

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV002313595

RCV002534560

ClinVar Variation:

588656

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135445.1:p.Val1044Met	CA636589 NM_001141973.3:c.3130G>A