Allele Registry

Canonical Allele Identifier: PA916028457

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009526

RCV000185840

RCV000202466

RCV000576348

RCV002496314

RCV003473067

RCV003934818

ClinVar Variation:

8964

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Pro227Leu	CA254612 NM_001330589.2:c.680C>T