{{Rsnum
|rsid=386134218
|Chromosome=5
|position=132392505
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SLC22A5
|Gene_s=SLC22A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=5
|CLNACC=RCV000022374.1
|CLNALLE=1
|CLNDBN=Renal carnitine transport defect
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK84551:C0342788:212140:158:21764004
|CLNHGVS=NC_000005.9:g.131728197A>G
|CLNSIG=5
|Disease=Renal carnitine transport defect
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=131728197
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386134218
|GENEINFO=SLC22A5:6584
|GENE_ID=6584
|GENE_NAME=SLC22A5
}}{{PMID Auto
|PMID=12408185
|Title=Identification of two novel mutations in OCTN2 from two Saudi patients with systemic carnitine deficiency.
}}