Allele Registry

Canonical Allele Identifier: PA2828781014

Gene: CPT1C HGNC NCBI

ClinVar Allele:

187089

ClinVar RCV:

RCV000169633

ClinVar Variation:

189198

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365411.1:p.Arg37Cys	CA199135 NM_001378482.1:c.109C>T