Allele Registry

Canonical Allele Identifier: PA344959

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV000055852

ClinVar Variation:

65639

HGVS (amino-acid)	Matching Registered Transcripts
NP_001027017.1:p.Phe343Val	CA344958 NM_001031847.3:c.1027T>G