Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.128485837G>CCA354406006GATA2c.761C>G (p.Pro254Arg)
c.1043C>G (p.Pro348Arg)
 ClinVar dbSNP gnomAD v4
3g.128485837G>ACA128576GATA2c.761C>T (p.Pro254Leu)
c.1043C>T (p.Pro348Leu)
 ClinVar dbSNP

Number of alleles fetched