Canonical Allele Identifier: PA891844829
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 568495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Val410Ile
CA859149
NM_000098.3:c.1228G>A