Allele Registry

Canonical Allele Identifier: PA101012

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009516

RCV000202437

RCV003473064

ClinVar Variation:

8957

HGVS (amino-acid)	Matching Registered Transcripts
NP_000089.1:p.Glu174Lys	CA254609 NM_000098.3:c.520G>A