Allele Registry

Canonical Allele Identifier: PA1139715043

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV001034856

ClinVar Variation:

834217

HGVS (amino-acid)	Matching Registered Transcripts
NP_001867.2:p.Phe765Leu	CA381624699 NM_001876.4:c.2295T>G CA381624700 NM_001876.4:c.2295T>A CA381624705 NM_001876.4:c.2293T>C