Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.25007438A>TCA213228ARXc.1121T>A (p.Val374Asp)
 ClinVar dbSNP
Xg.25007438A>CCA412611689ARXc.1121T>G (p.Val374Gly)
 dbSNP

Number of alleles fetched