Allele Registry

Canonical Allele Identifier: PA2825835641

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV003812688

ClinVar Variation:

2952001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135445.1:p.Val845Leu	CA18628836 NM_001141973.3:c.2533G>C