Allele Registry

Canonical Allele Identifier: PA2825835996

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000116443

RCV000675887

RCV001087148

RCV002312033

ClinVar Variation:

128474

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135445.1:p.Ala1139Thr	CA151961 NM_001141973.3:c.3415G>A