Allele Registry

Canonical Allele Identifier: PA101128

Gene: CPT2 HGNC NCBI

ClinVar RCV:

RCV000009514

RCV000202449

RCV000415611

ClinVar Variation:

8956

HGVS (amino-acid)	Matching Registered Transcripts
NP_000089.1:p.Tyr628Ser	CA254608 NM_000098.3:c.1883A>C