Canonical Allele Identifier: PA2825067661
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709821
ClinVar RCV Id: RCV002290163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Ser401Arg
CA340394732
NM_000098.3:c.1201A>C
CA340394737
NM_000098.3:c.1203C>A
CA340394738
NM_000098.3:c.1203C>G