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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
9
g.130862977A>T
CA16602552
ABL1
c.821A>T (p.Glu274Val)
c.764A>T (p.Glu255Val)
ClinVar
dbSNP
COSMIC
9
g.130862977A=
CA1881463524
ABL1
c.821A= (p.Glu274=)
c.764A= (p.Glu255=)
dbSNP
Number of alleles fetched
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