Allele Registry

Canonical Allele Identifier: PA916028447

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009516

RCV000202437

RCV003473064

ClinVar Variation:

8957

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Glu174Lys	CA254609 NM_001330589.2:c.520G>A