{{Rsnum
|rsid=119455957
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=TPP1
|position=6616696
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPP1
}}{{omim
|id=607998
|rsnum=119455957
|variant=0007
}}{{ClinVar
|rsid=119455957
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=6637927
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=TPP1:1200
|GENE_NAME=TPP1
|GENE_ID=1200
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.6637927C>A
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=607998.0007; VAR_016795
|CLNSIG=5
|CLNCUI=C1876161
|CLNDBN=Ceroid lipofuscinosis, neuronal, 2
|Disease=Ceroid lipofuscinosis
|CLNACC=RCV000002766.3
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1876161:204500:168491:228349:79264
}}{{PMID Auto
|PMID=11339651
|Title=Heterogeneity of late-infantile neuronal ceroid lipofuscinosis.
}}

{{PMID Auto
|PMID=12414822
|Title=Identification of novel CLN2 mutations shows Canadian specific NCL2 alleles.
|OA=1
}}