Canonical Allele Identifier: PA916028498
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 568495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Val410Ile
CA859149
NM_001330589.2:c.1228G>A