Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.70028006C>TCA273141EDAc.676C>T (p.Gln226Ter)
c.280C>T (p.Gln94Ter)
 ClinVar dbSNP gnomAD v4
Xg.70028006C=CA2435979605EDAc.676C= (p.Gln226=)
c.280C= (p.Gln94=)
 dbSNP

Number of alleles fetched