Canonical Allele Identifier: PA2573200990
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1370451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Arg382Thr
CA859135
NM_001330589.2:c.1145G>C