Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904998C>TCA255162F8c.5399G>A (p.Arg1800His)
c.5294G>A (p.Arg1765His)
 ClinVar dbSNP gnomAD v4
Xg.154904998C=CA2466828475F8c.5399G= (p.Arg1800=)
c.5294G= (p.Arg1765=)
 dbSNP

Number of alleles fetched