Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.63495972C>TCA150649EEF1A2c.208G>A (p.Gly70Ser)
n.2777G>A
c.*80G>A (n.*80G>A)
 ClinVar dbSNP
20g.63495972C=CA2374824109EEF1A2c.208G= (p.Gly70=)
n.2777G=
c.*80G= (n.*80G=)
 dbSNP

Number of alleles fetched