Canonical Allele Identifier: PA2573200793
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685671
ClinVar RCV Id: RCV002249838

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317518.1:p.Leu178_Pro180delinsPhe
CA859002
NM_001330589.2:c.534_539del