Allele Registry

Canonical Allele Identifier: PA2825814826

Gene: CPT1C HGNC NCBI

ClinVar RCV:

RCV000542129

ClinVar Variation:

476175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129524.1:p.Asn687Asp	CA9582408 NM_001136052.3:c.2059A>G