Allele Registry

Canonical Allele Identifier: PA2825835664

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000056336

ClinVar Variation:

66099

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135445.1:p.Gly872Arg	CA264800 NM_001141973.3:c.2614G>A CA338238915 NM_001141973.3:c.2614G>C