Allele Registry

Canonical Allele Identifier: PA270166

Gene: ATP13A2 HGNC NCBI

ClinVar Allele:

152914

ClinVar RCV:

RCV000132730

RCV001857477

RCV003114286

ClinVar Variation:

143196

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Arg164Trp	CA270165 NM_022089.4:c.490C>T