Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119676851C>TCA346200BAG3c.1297C>T (p.Gln433Ter)
c.1294C>T (p.Gln432Ter)
 ClinVar dbSNP
10g.119676851C=CA1940196731BAG3c.1297C= (p.Gln433=)
c.1294C= (p.Gln432=)
 dbSNP

Number of alleles fetched