Allele Registry

Canonical Allele Identifier: PA2825836680

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000415515

ClinVar Variation:

374888

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135446.1:p.Thr512Ile	CA16043959 NM_001141974.3:c.1535C>T