Allele Registry

Canonical Allele Identifier: PA2825358270

Gene: CPT1A HGNC NCBI

ClinVar RCV:

RCV002043758

ClinVar Variation:

1519665

HGVS (amino-acid)	Matching Registered Transcripts
NP_001027017.1:p.Phe462Leu	CA381630830 NM_001031847.3:c.1386C>G CA381630831 NM_001031847.3:c.1386C>A CA381630836 NM_001031847.3:c.1384T>C