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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
13
g.32339152del
CA020842
BRCA2
c.4797del (p.Asn1599LysfsTer18)
c.4428del (p.Asn1476LysfsTer18)
n.4797del
ClinVar
dbSNP
13
g.32339152T=
CA2082815934
BRCA2
c.4797T= (p.Asn1599=)
c.4428T= (p.Asn1476=)
n.4797T=
dbSNP
dbSNP
Number of alleles fetched
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