Allele Registry

Canonical Allele Identifier: PA916028429

Gene: CPT2 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000009510

RCV000185836

RCV000194764

RCV000202499

RCV000515252

RCV000576571

RCV000624845

RCV000662284

RCV001004157

RCV001813968

RCV003137507

ClinVar Variation:

8953

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Ser113Leu	CA254605 NM_001330589.2:c.338C>T