Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.119278238G>CCA382912659CBLc.*620G>C (n.*620G>C)
c.1168G>C (p.Asp390His)
c.1162G>C (p.Asp388His)
ClinVar dbSNP
11g.119278238G>TCA123488CBLc.*620G>T (n.*620G>T)
c.1168G>T (p.Asp390Tyr)
c.1162G>T (p.Asp388Tyr)
ClinVar dbSNP
11g.119278238G>ACA382912657CBLc.*620G>A (n.*620G>A)
c.1168G>A (p.Asp390Asn)
c.1162G>A (p.Asp388Asn)
dbSNP

Number of alleles fetched