Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.36291990T>CCA411381860MYH9c.4403A>G (p.Asp1468Gly)
n.4635A>G
c.4340A>G (p.Asp1447Gly)
 ClinVar dbSNP
22g.36291990T>ACA347309MYH9c.4403A>T (p.Asp1468Val)
n.4635A>T
c.4340A>T (p.Asp1447Val)
 ClinVar dbSNP

Number of alleles fetched