Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904867G>ACA255170F8c.5530C>T (p.Pro1844Ser)
c.5425C>T (p.Pro1809Ser)
 ClinVar dbSNP
Xg.154904867G=CA2466828433F8c.5530C= (p.Pro1844=)
c.5425C= (p.Pro1809=)
 dbSNP

Number of alleles fetched