{{Rsnum
|rsid=119455958
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TPP1
|position=6616690
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPP1
}}{{omim
|id=607998
|rsnum=119455958
|variant=0008
}}{{ClinVar
|rsid=119455958
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=6637921
|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.6637921T>C
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=607998.0008; VAR_016796
|CLNSIG=5
|CLNCUI=C1876161
|CLNDBN=Ceroid lipofuscinosis, neuronal, 2
|Disease=Ceroid lipofuscinosis
|CLNACC=RCV000002767.2
|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=12376936
|Title=Late infantile neuronal ceroid lipofuscinosis: quantitative description of the clinical course in patients with CLN2 mutations.
}}