Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.134377751G>ACA121326PHF6c.134G>A (p.Cys45Tyr)
n.307G>A
ClinVar dbSNP
Xg.134377751G=CA2459705546PHF6c.134G= (p.Cys45=)
n.307G=
dbSNP

Number of alleles fetched