Allele Registry

Canonical Allele Identifier: PA658830127

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV000666810

ClinVar Variation:

551684

HGVS (amino-acid)	Matching Registered Transcripts
NP_001867.2:p.Gly465Arg	CA6152314 NM_001876.4:c.1393G>A CA381630813 NM_001876.4:c.1393G>C