Allele Registry

Canonical Allele Identifier: PA2827333204

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009514

RCV000202449

RCV000415611

ClinVar Variation:

8956

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317518.1:p.Tyr605Ser	CA254608 NM_001330589.2:c.1814A>C