Allele Registry

Canonical Allele Identifier: PA2827333209

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009508

RCV000202472

RCV000415574

RCV001781211

RCV002476950

RCV003473062

ClinVar Variation:

8952

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Arg608Cys	CA254604 NM_001330589.2:c.1822C>T