Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908784G>CCA127524APOEc.488G>C (p.Arg163Pro)
c.566G>C (p.Arg189Pro)
ClinVar dbSNP
19g.44908784G>ACA127513APOEc.488G>A (p.Arg163His)
c.566G>A (p.Arg189His)
ClinVar dbSNP gnomAD

Number of alleles fetched