Allele Registry

Canonical Allele Identifier: PA109919

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000056335

ClinVar Variation:

66098

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Met854Arg	CA264798 NM_022089.4:c.2561T>G