{{Rsnum
|rsid=80356796
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CPT1A
|Gene_s=CPT1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=68793336
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNALLE=1
|CLNDBN=Carnitine palmitoyltransferase I deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1527:C0342789:255120:156:238001003
|CLNHGVS=NC_000011.9:g.68560804G>C
|CLNORIGIN=0
|CLNSIG=5
|Disease=Carnitine palmitoyltransferase I deficiency
|FwdALT=G
|FwdREF=C
|GENEINFO=CPT1A:1374
|GENE_ID=1374
|GENE_NAME=CPT1A
|REF=G
|RSPOS=68560804
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80356796
|CLNACC=RCV000055872.1
|CLNSRC=GeneReviews
|CLNSRCID=NBK1527
}}{{PMID Auto
|PMID=15110323
|Title=Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency.
}}