{{Rsnum
|rsid=80356784
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=CPT1A
|Gene_s=CPT1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=68780705
}}{{ClinVar
|ALT=A
|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.68548173C>A
|CLNORIGIN=0
|CLNSIG=5
|Disease=Carnitine palmitoyltransferase I deficiency
|FwdALT=T
|FwdREF=G
|GENEINFO=CPT1A:1374
|GENE_ID=1374
|GENE_NAME=CPT1A
|REF=C
|RSPOS=68548173
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000000000002110100
|WGT=0
|dbSNPBuildID=131
|rsid=80356784
|CLNACC=RCV000055855.1
|CLNSRC=GeneReviews
|CLNSRCID=NBK1527
}}{{PMID Auto
|PMID=15110323
|Title=Novel mutations in CPT 1A define molecular heterogeneity of hepatic carnitine palmitoyltransferase I deficiency.
}}