Canonical Allele Identifier: PA2825358013
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2040969
ClinVar RCV Id: RCV002912807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Thr300Met
CA6152485
NM_001031847.3:c.899C>T