Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.64805078A>TCA009116MEN1c.1321T>A (p.Trp441Arg)
c.1306T>A (p.Trp436Arg)
c.1432T>A (p.Trp478Arg)
c.1447T>A (p.Trp483Arg)
c.1201T>A (p.Trp401Arg)
c.1186-262T>A (p.=)
n.855T>A
ClinVar dbSNP
11g.64805078A>GCA223912292MEN1c.1321T>C (p.Trp441Arg)
c.1306T>C (p.Trp436Arg)
c.1432T>C (p.Trp478Arg)
c.1447T>C (p.Trp483Arg)
c.1201T>C (p.Trp401Arg)
c.1186-262T>C (p.=)
n.855T>C
ClinVar dbSNP

Number of alleles fetched