Allele Registry

Canonical Allele Identifier: PA2825837317

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000415585

ClinVar Variation:

374887

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135446.1:p.Phe1007del	CA16043958 NM_001141974.3:c.3020_3022del