Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908645G>ACA042275APOEc.349G>A (p.Ala117Thr)
c.427G>A (p.Ala143Thr)
 ClinVar dbSNP
19g.44908645G=CA2338167460APOEc.349G= (p.Ala117=)
c.427G= (p.Ala143=)
 dbSNP

Number of alleles fetched