Canonical Allele Identifier: PA658804502
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 529863
ClinVar RCV Id: RCV000635365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Leu170Arg
CA22637761
NM_000098.3:c.509T>G
CA658795466
NM_000098.3:c.509_510delinsGC