Allele Registry

Canonical Allele Identifier: PA2828781612

Gene: CPT1C HGNC NCBI

ClinVar RCV:

RCV000653259

RCV003907915

RCV004025900

ClinVar Variation:

542768

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365413.1:p.Pro687Ala	CA9582404 NM_001378484.1:c.2059C>G