Allele Registry

Canonical Allele Identifier: PA109897

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000056336

ClinVar Variation:

66099

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Gly877Arg	CA264800 NM_022089.4:c.2629G>A CA338238915 NM_022089.4:c.2629G>C