Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.25897619G>ACA258118APPn.1985C>T
n.415C>T
n.684C>T
c.2018C>T (p.Ala673Val)
c.1793C>T (p.Ala598Val)
c.1625C>T (p.Ala542Val)
c.1961C>T (p.Ala654Val)
c.1964C>T (p.Ala655Val)
c.1688C>T (p.Ala563Val)
c.1850C>T (p.Ala617Val)
c.1946C>T (p.Ala649Val)
n.365C>T
c.1907C>T (p.Ala636Val)
c.1739C>T (p.Ala580Val)
ClinVar dbSNP
21g.25897619G>CCA409806410APPn.1985C>G
n.415C>G
n.684C>G
c.2018C>G (p.Ala673Gly)
c.1793C>G (p.Ala598Gly)
c.1625C>G (p.Ala542Gly)
c.1961C>G (p.Ala654Gly)
c.1964C>G (p.Ala655Gly)
c.1688C>G (p.Ala563Gly)
c.1850C>G (p.Ala617Gly)
c.1946C>G (p.Ala649Gly)
n.365C>G
c.1907C>G (p.Ala636Gly)
c.1739C>G (p.Ala580Gly)
dbSNP

Number of alleles fetched