Canonical Allele Identifier: PA2499249768
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015254
ClinVar RCV Id: RCV001314084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Glu386Ala
CA340394638
NM_001330589.2:c.1157A>C