Allele Registry

Canonical Allele Identifier: PA100086

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV000055872

RCV000298507

ClinVar Variation:

65659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001867.2:p.Arg316Gly	CA344991 NM_001876.4:c.946C>G