Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.129528800C>TCA354495494RHOc.67C>T (p.Pro23Ser)
ClinVar dbSNP
3g.129528800C>GCA256695RHOc.67C>G (p.Pro23Ala)
ClinVar dbSNP
3g.129528800C>ACA354495488RHOc.67C>A (p.Pro23Thr)
ClinVar dbSNP
3g.129528800C=CA1401205150RHOc.67C= (p.Pro23=)
dbSNP

Number of alleles fetched