Canonical Allele Identifier: PA645421006
Gene: CPT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000089.1:p.Met307Ile
CA859081
NM_000098.3:c.921G>A
CA340394123
NM_000098.3:c.921G>C
CA340394124
NM_000098.3:c.921G>T