Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.32338694delCA020014BRCA2c.4339del (p.Val1447Ter)
c.3970del (p.Val1324Ter)
n.4339del
 ClinVar dbSNP
13g.32338694G=CA2082810824BRCA2c.4339G= (p.Val1447=)
c.3970G= (p.Val1324=)
n.4339G=
 dbSNP dbSNP

Number of alleles fetched