{{Rsnum
|rsid=121434286
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CLN3
|position=28482500
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CLN3
}}{{omim
|id=607042
|rsnum=121434286
|variant=0005
}}{{ClinVar
|rsid=121434286
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=28493821
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=CLN3:1201
|GENE_NAME=CLN3
|GENE_ID=1201
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.28493821C>A; NC_000016.9:g.28493821C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNACC=RCV000049702.1; RCV000003735.1; RCV000055839.1
|CLNDBN=Juvenile neuronal ceroid lipofuscinosis; Ceroid lipofuscinosis, neuronal, 3, protracted
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1428:C0751383:204200:228346:79264:61663001
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1428; 607042.0005
|Disease=Juvenile neuronal ceroid lipofuscinosis; Ceroid lipofuscinosis
}}{{PMID Auto
|PMID=21990111
|Title=Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses.
}}