Allele Registry

Canonical Allele Identifier: PA100950

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009519

RCV000202513

RCV001004160

RCV002490348

RCV003317032

RCV003450624

RCV003473066

ClinVar Variation:

8959

HGVS (amino-acid)	Matching Registered Transcripts
NP_000089.1:p.Arg503Cys	CA120021 NM_000098.3:c.1507C>T