{{Rsnum
|rsid=386833700
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CLN3
|position=28491502
|Gene_s=CLN3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000049661.1
|CLNALLE=1
|CLNDBN=Juvenile neuronal ceroid lipofuscinosis
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1428:C0751383:204200:228346:79264:61663001
|CLNHGVS=NC_000016.9:g.28502823C>T
|CLNSIG=4
|Disease=Juvenile neuronal ceroid lipofuscinosis
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=28502823
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833700
|GENEINFO=CLN3:1201
|GENE_ID=1201
|GENE_NAME=CLN3
}}{{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.
}}