{{Rsnum
|rsid=80356533
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP1A3
|position=41985082
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ATP1A3
}}{{omim
|id=182350
|rsnum=80356533
|variant=0003
}}{{ClinVar
|rsid=80356533
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=42489234
|CHROM=19
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=ATP1A3:478
|GENE_NAME=ATP1A3
|GENE_ID=478
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.42489234C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1115; 182350.0003
|CLNSIG=5
|CLNCUI=C1868681; C1868681
|CLNDBN=Dystonia 12
|Disease=Dystonia 12
|CLNACC=RCV000013774.23
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1115:C1868681:128235:71517
}}{{PMID Auto
|PMID=15260953
|Title=Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
}}

{{PMID Auto
|PMID=17282997
|Title=The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
}}