Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.114716124C>GCA151261NRASc.37G>C (p.Gly13Arg)
ClinVar dbSNP gnomAD v4 COSMIC
1g.114716124C>ACA16602248NRASc.37G>T (p.Gly13Cys)
ClinVar dbSNP gnomAD v4 COSMIC
1g.114716124C>TCA16602674NRASc.37G>A (p.Gly13Ser)
ClinVar dbSNP COSMIC
1g.114716124C=CA1141580992NRASc.37G= (p.Gly13=)
dbSNP

Number of alleles fetched