Canonical Allele Identifier: PA2825067365
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1437973
ClinVar RCV Id: RCV001948862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Ser230Arg
CA340393288
NM_000098.3:c.688A>C
CA340393304
NM_000098.3:c.690T>A
CA340393305
NM_000098.3:c.690T>G