Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154903951G>ACA255191F8c.5953C>T (p.Arg1985Ter)
c.5848C>T (p.Arg1950Ter)
ClinVar dbSNP COSMIC COSMIC
Xg.154903951G>CCA414905720F8c.5953C>G (p.Arg1985Gly)
c.5848C>G (p.Arg1950Gly)
ClinVar dbSNP
Xg.154903951G=CA2466828148F8c.5953C= (p.Arg1985=)
c.5848C= (p.Arg1950=)
dbSNP

Number of alleles fetched