Canonical Allele Identifier: PA2825358005
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1693056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Arg295Cys
CA381634307
NM_001031847.3:c.883C>T