Allele Registry

Canonical Allele Identifier: PA2827333052

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009513

RCV000675130

ClinVar Variation:

8955

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Asp530Asn	CA254607 NM_001330589.2:c.1588G>A