Allele Registry

Canonical Allele Identifier: PA264799

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000056335

ClinVar Variation:

66098

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135446.1:p.Met810Arg	CA264798 NM_001141974.3:c.2429T>G