Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130872902T>GCA16602579ABL1c.1007T>G (p.Phe336Cys)
c.950T>G (p.Phe317Cys)
ClinVar dbSNP
9g.130872902T=CA1881476025ABL1c.1007T= (p.Phe336=)
c.950T= (p.Phe317=)
dbSNP

Number of alleles fetched