Canonical Allele Identifier: PA916028499
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 576519
ClinVar RCV Id: RCV000699030 RCV003480783
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Thr411Met
CA859151
NM_001330589.2:c.1232C>T