Canonical Allele Identifier: PA2825358173
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2199202
ClinVar RCV Id: RCV002634199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Val389Ile
CA6152375
NM_001031847.3:c.1165G>A