Canonical Allele Identifier: PA2580260235
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2199202
ClinVar RCV Id: RCV002634199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Val389Ile
CA6152375
NM_001876.4:c.1165G>A