Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.68780737T>CCA340848CPT1Ac.1361A>G (p.Asp454Gly)
c.1457A>G (p.Asp486Gly)
 ClinVar dbSNP
11g.68780737T=CA3182674347CPT1Ac.1361A= (p.Asp454=)
c.1457A= (p.Asp486=)
 dbSNP

Number of alleles fetched