Allele Registry

Canonical Allele Identifier: PA100967

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009508

RCV000202472

RCV000415574

RCV001781211

RCV002476950

RCV003473062

ClinVar Variation:

8952

HGVS (amino-acid)	Matching Registered Transcripts
NP_000089.1:p.Arg631Cys	CA254604 NM_000098.3:c.1891C>T