Canonical Allele Identifier: PA916028497
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 297606
ClinVar RCV Id: RCV000405294

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Glu386Asp
CA859137
NM_001330589.2:c.1158A>C
CA340394641
NM_001330589.2:c.1158A>T