{{Rsnum
|rsid=387907281
|Chromosome=19
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP1A3
|position=41970284
|Gene_s=ATP1A3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=19
|CLNACC=RCV000030750.16
|CLNALLE=1
|CLNDBN=Alternating hemiplegia of childhood 2
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN143722:614820:2131
|CLNHGVS=NC_000019.9:g.42474436C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=182350.0010
|Disease=Alternating hemiplegia of childhood 2
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=42474436
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907281
|GENEINFO=ATP1A3:478
|GENE_ID=478
|GENE_NAME=ATP1A3
}}