Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47410322T>CCA021524MSH2c.595T>C (p.Cys199Arg)
c.397T>C (p.Cys133Arg)
n.667T>C
n.657T>C
 ClinVar dbSNP COSMIC
2g.47410322T>GCA346731038MSH2c.595T>G (p.Cys199Gly)
c.397T>G (p.Cys133Gly)
n.667T>G
n.657T>G
 ClinVar dbSNP

Number of alleles fetched