Allele Registry

Canonical Allele Identifier: PA100989

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009513

RCV000675130

ClinVar Variation:

8955

HGVS (amino-acid)	Matching Registered Transcripts
NP_000089.1:p.Asp553Asn	CA254607 NM_000098.3:c.1657G>A