Allele Registry

Canonical Allele Identifier: PA276127

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000191065

RCV002514094

ClinVar Variation:

209136

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Gly315Arg	CA276126 NM_022089.4:c.943G>A CA338257126 NM_022089.4:c.943G>C