Canonical Allele Identifier: PA340861
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 9069
ClinVar RCV Id: RCV000009636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Gly709Glu
CA340860
NM_001031847.3:c.2126G>A