ClinGen Allele Registry
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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
9
g.130862955C>G
CA16602546
ABL1
c.799C>G (p.Leu267Val)
c.742C>G (p.Leu248Val)
ClinVar
dbSNP
COSMIC
9
g.130862955C>A
CA375263219
ABL1
c.799C>A (p.Leu267Met)
c.742C>A (p.Leu248Met)
dbSNP
Number of alleles fetched
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