Allele Registry

Canonical Allele Identifier: PA916028496

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009517

RCV000009518

RCV000202462

RCV000411002

RCV000762943

RCV001004159

RCV001270097

RCV003473065

ClinVar Variation:

8958

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Phe383Tyr	CA254610 NM_001330589.2:c.1148T>A