Allele Registry

Canonical Allele Identifier: PA109887

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000001280

RCV001851533

RCV002251851

ClinVar Variation:

1221

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Gly504Arg	CA251716 NM_022089.4:c.1510G>C CA338251861 NM_022089.4:c.1510G>A