Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.35245020G>ACA116974TBX20c.583C>T (p.Gln195Ter)
n.594C>T
c.-15C>T (n.-15C>T)
 ClinVar dbSNP
7g.35245020G=CA1699584631TBX20c.583C= (p.Gln195=)
n.594C=
c.-15C= (n.-15C=)
 dbSNP

Number of alleles fetched