Allele Registry

Canonical Allele Identifier: PA151962

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000116443

RCV000675887

RCV001087148

RCV002312033

ClinVar Variation:

128474

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Ala1144Thr	CA151961 NM_022089.4:c.3430G>A