Canonical Allele Identifier: PA2825067632
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2188458
ClinVar RCV Id: RCV002620243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Val380Leu
CA859133
NM_000098.3:c.1138G>C
CA340394597
NM_000098.3:c.1138G>T