Allele Registry

Canonical Allele Identifier: PA2825067592

Gene: CPT2 HGNC NCBI

ClinVar Variation Id: 944068

HGVS (amino-acid)	Matching Registered Transcripts
NP_000089.1:p.Phe352Leu	CA859116 NM_000098.3:c.1054T>C CA340394416 NM_000098.3:c.1056T>A CA340394417 NM_000098.3:c.1056T>G