Canonical Allele Identifier: PA645421046
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 297606
ClinVar RCV Id: RCV000405294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Glu386Asp
CA859137
NM_000098.3:c.1158A>C
CA340394641
NM_000098.3:c.1158A>T