Allele Registry

Canonical Allele Identifier: PA2825836672

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000001280

RCV001851533

RCV002251851

ClinVar Variation:

1221

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135446.1:p.Gly499Arg	CA251716 NM_001141974.3:c.1495G>C CA338251861 NM_001141974.3:c.1495G>A