Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44909171G>ACA127519APOEc.875G>A (p.Arg292His)
c.953G>A (p.Arg318His)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.44909171G>TCA406305731APOEc.875G>T (p.Arg292Leu)
c.953G>T (p.Arg318Leu)
 dbSNP gnomAD v4 COSMIC

Number of alleles fetched