Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.47566721T>GCA16602806ARAFc.640T>G (p.Ser214Ala)
c.649T>G (p.Ser217Ala)
c.655T>G (p.Ser219Ala)
c.-18T>G (n.-18T>G)
ClinVar dbSNP COSMIC
Xg.47566721T>ACA412813391ARAFc.640T>A (p.Ser214Thr)
c.649T>A (p.Ser217Thr)
c.655T>A (p.Ser219Thr)
c.-18T>A (n.-18T>A)
dbSNP COSMIC

Number of alleles fetched