Canonical Allele Identifier: PA2825357721
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2157873
ClinVar RCV Id: RCV003078318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Ala94Val
CA6152730
NM_001031847.3:c.281C>T