Canonical Allele Identifier: PA1139714684
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 970963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Val179Ile
CA6152632
NM_001876.4:c.535G>A