Allele Registry

Canonical Allele Identifier: PA2573200792

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV002033420

RCV002497967

RCV003453924

RCV003453925

RCV003453926

RCV003456268

ClinVar Variation:

1486923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Glu174Gln	CA340392451 NM_001330589.2:c.520G>C