Allele Registry

Canonical Allele Identifier: PA2825837073

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000056336

ClinVar Variation:

66099

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135446.1:p.Gly833Arg	CA264800 NM_001141974.3:c.2497G>A CA338238915 NM_001141974.3:c.2497G>C