Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.5955211C>GCA214559MCM8c.446C>G (p.Pro149Arg)
n.786C>G
c.254C>G (p.Pro85Arg)
 ClinVar dbSNP
20g.5955211C=CA2347739081MCM8c.446C= (p.Pro149=)
n.786C=
c.254C= (p.Pro85=)
 dbSNP

Number of alleles fetched