Canonical Allele Identifier: PA2825358008
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2140825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Gly298Arg
CA6152488
NM_001031847.3:c.892G>A
CA381634290
NM_001031847.3:c.892G>C