Canonical Allele Identifier: PA1139714789
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 985485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Arg395Pro
CA381631932
NM_001876.4:c.1184G>C