Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.36295069G>ACA257087MYH9c.3556C>T (p.Arg1186Cys)
n.3788C>T
c.3493C>T (p.Arg1165Cys)
 ClinVar dbSNP
22g.36295069G=CA2403801543MYH9c.3556C= (p.Arg1186=)
n.3788C=
c.3493C= (p.Arg1165=)
 dbSNP

Number of alleles fetched