{{Rsnum
|rsid=80356790
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CPT1A
|position=68781882
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CPT1A
}}{{omim
|id=600528
|rsnum=80356790
|variant=0004
}}{{ClinVar
|rsid=80356790
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=68549350
|CHROM=11
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=CPT1A:1374
|GENE_NAME=CPT1A
|GENE_ID=1374
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.68549350G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1527; 600528.0004
|CLNSIG=5
|CLNCUI=C0342789
|CLNDBN=Carnitine palmitoyltransferase I deficiency
|Disease=Carnitine palmitoyltransferase I deficiency
|CLNACC=RCV000009632.2
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1527:C0342789:255120:156:238001003
}}{{PMID|12189492}} Organization of the human liver carnitine palmitoyltransferase 1 gene ( CPT1A) and identification of novel mutations in hypoketotic hypoglycaemia.

{{PMID|14517221}} Functional and structural basis of carnitine palmitoyltransferase 1A deficiency.