Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154906457C>TCA255161F8c.5336G>A (p.Gly1779Glu)
c.5231G>A (p.Gly1744Glu)
 ClinVar dbSNP
Xg.154906457C=CA2466828922F8c.5336G= (p.Gly1779=)
c.5231G= (p.Gly1744=)
 dbSNP

Number of alleles fetched