Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32337624delCA017683BRCA2c.3269del (p.Met1090SerfsTer14)
c.2900del (p.Met967SerfsTer14)
n.3269del
 ClinVar dbSNP
13g.32337624T=CA3200672644BRCA2c.3269T= (p.Met1090=)
c.2900T= (p.Met967=)
n.3269T=
 dbSNP dbSNP

Number of alleles fetched