Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.119676939T>CCA261131BAG3c.1385T>C (p.Leu462Pro)
c.1382T>C (p.Leu461Pro)
 ClinVar dbSNP
10g.119676939T=CA1940196768BAG3c.1385T= (p.Leu462=)
c.1382T= (p.Leu461=)
 dbSNP

Number of alleles fetched