Canonical Allele Identifier: PA1139714729
Gene: CPT1A HGNC NCBI

Linked Data

ClinVar Variation Id: 990117
ClinVar RCV Id: RCV001278064 RCV003166603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001867.2:p.Gly298Val
CA381634286
NM_001876.4:c.893G>T