Canonical Allele Identifier: PA101012
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Glu174Lys
CA254609
NM_000098.3:c.520G>A