Canonical Allele Identifier: PA891844830
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 576519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Thr411Met
CA859151
NM_000098.3:c.1232C>T