Canonical Allele Identifier: PA145734
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 92428

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Phe352Cys
CA145733
NM_000098.3:c.1055T>G