Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904004C>TCA255188F8c.5900G>A (p.Gly1967Asp)
c.5795G>A (p.Gly1932Asp)
 ClinVar dbSNP
Xg.154904004C=CA2466828165F8c.5900G= (p.Gly1967=)
c.5795G= (p.Gly1932=)
 dbSNP

Number of alleles fetched