Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129532722A>GCA256677RHOc.886A>G (p.Lys296Glu)
ClinVar dbSNP
3g.129532722A>CCA354470787RHOc.886A>C (p.Lys296Gln)
ClinVar dbSNP
3g.129532722A=CA1401211987RHOc.886A= (p.Lys296=)
dbSNP

Number of alleles fetched