Canonical Allele Identifier: PA916028426
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 460433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Lys79Thr
CA858937
NM_001330589.2:c.236A>C