Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.59024206T>CCA16043139TUBB1c.779T>C (p.Phe260Ser)
c.713T>C (p.Phe238Ser)
ClinVar dbSNP gnomAD v4
20g.59024206T=CA2372582122TUBB1c.779T= (p.Phe260=)
c.713T= (p.Phe238=)
dbSNP

Number of alleles fetched