Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32339759C>TCA022246BRCA2c.5404C>T (p.Gln1802Ter)
c.5035C>T (p.Gln1679Ter)
n.5404C>T
 ClinVar dbSNP
13g.32339759C=CA2082822912BRCA2c.5404C= (p.Gln1802=)
c.5035C= (p.Gln1679=)
n.5404C=
 dbSNP

Number of alleles fetched