Canonical Allele Identifier: PA2825357666
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1918334
ClinVar RCV Id: RCV002625807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Thr71Ala
CA381638051
NM_001031847.3:c.211A>G