Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25013000C>ACA213238ARXc.995G>T (p.Arg332Leu)
 ClinVar dbSNP
Xg.25013000C>TCA213168ARXc.995G>A (p.Arg332His)
 ClinVar dbSNP gnomAD v4
Xg.25013000C=CA2420209081ARXc.995G= (p.Arg332=)
 dbSNP

Number of alleles fetched