{{Rsnum
|rsid=80338726
|Chromosome=7
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=SLC25A13
|position=96121696
|Gene_s=SLC25A13
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GT
|CHROM=7
|CLNACC=RCV000006374.2; RCV000006375.2
|CLNALLE=1
|CLNDBN=Citrullinemia type II; Neonatal intrahepatic cholestasis caused by citrin deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1181:C1863844:603471:247585; NBK1181:C1853942:605814:247598
|CLNHGVS=NC_000007.13:g.95751009dupT
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1181; 603859.0006
|Disease=Citrullinemia type II; Neonatal intrahepatic cholestasis caused by citrin deficiency
|FwdALT=A
|GENEINFO=SLC25A13:10165
|GENE_ID=10165
|GENE_NAME=SLC25A13
|REF=G
|RSPOS=95751008
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050168000000000002110200
|WGT=0
|dbSNPBuildID=131
|rsid=80338726
}}{{PMID Auto
|PMID=11153906
|Title=Identification of two novel mutations in the SLC25A13 gene and detection of seven mutations in 102 patients with adult-onset type II citrullinemia.
}}