Allele Registry

Canonical Allele Identifier: PA2825835648

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000056335

ClinVar Variation:

66098

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135445.1:p.Met849Arg	CA264798 NM_001141973.3:c.2546T>G