Allele Registry

Canonical Allele Identifier: PA2741858673

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV003740855

ClinVar Variation:

2904999

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Asp213Ala	CA340393017 NM_001330589.2:c.638A>C