Canonical Allele Identifier: PA658804504
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 529867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Ser293Gly
CA859067
NM_000098.3:c.877A>G