Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25012997G>TCA121411ARXc.998C>A (p.Thr333Asn)
 ClinVar dbSNP gnomAD v4
Xg.25012997G>CCA171168ARXc.998C>G (p.Thr333Ser)
 ClinVar dbSNP
Xg.25012997G=CA2420209080ARXc.998C= (p.Thr333=)
 dbSNP

Number of alleles fetched