{{Rsnum
|rsid=386134183
|Chromosome=2
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AT)
|geno3=(AT;AT)
|Gene=ALS2
|position=201733318
|Gene_s=ALS2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=2
|CLNACC=RCV000004660.3
|CLNALLE=1
|CLNDBN=Infantile-onset ascending hereditary spastic paralysis
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1243:C1846588:607225:293168
|CLNHGVS=NC_000002.11:g.202598041_202598042delAT
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1243; 606352.0007
|Disease=Infantile-onset ascending hereditary spastic paralysis
|FwdREF=AT
|REF=AAT
|RSPOS=202598040
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386134183
|GENEINFO=ALS2:57679
|GENE_ID=57679
|GENE_NAME=ALS2
}}{{PMID Auto
|PMID=12145748
|Title=Infantile-onset ascending hereditary spastic paralysis is associated with mutations in the alsin gene.
|OA=1
}}