Canonical Allele Identifier: PA2573200887
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1362426
ClinVar RCV Id: RCV001900172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Ile263Thr
CA859048
NM_001330589.2:c.788T>C