Canonical Allele Identifier: PA2825357677
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 1010287
ClinVar RCV Id: RCV001307893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027017.1:p.Tyr74_Ser80del
CA2497319869
NM_001031847.3:c.221_241del