Canonical Allele Identifier: PA916028485
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Met342Thr
CA859108
NM_001330589.2:c.1025T>C