Allele Registry

Canonical Allele Identifier: PA916028493

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000078116

RCV000202483

RCV000711317

RCV001533571

RCV001533572

RCV003974955

ClinVar Variation:

92429

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Val368Ile	CA285313 NM_001330589.2:c.1102G>A