Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.6019502G>TCA478502941VWFc.3916C>A (p.Arg1306=)
n.421-25568C>A
 dbSNP gnomAD v4
12g.6019502G>ACA114123VWFc.3916C>T (p.Arg1306Trp)
n.421-25568C>T
 ClinVar dbSNP

Number of alleles fetched