Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.4110564C>GCA403391425MAP2K2n.834G>C
c.395G>C (p.Gly132Ala)
c.104G>C (p.Gly35Ala)
n.592G>C
dbSNP
19g.4110564C>TCA250288MAP2K2n.834G>A
c.395G>A (p.Gly132Asp)
c.104G>A (p.Gly35Asp)
n.592G>A
ClinVar dbSNP
19g.4110564C>ACA403391424MAP2K2n.834G>T
c.395G>T (p.Gly132Val)
c.104G>T (p.Gly35Val)
n.592G>T
ClinVar dbSNP

Number of alleles fetched