Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.6021960C>ACA228427VWFc.3614G>T (p.Arg1205Leu)
ClinVar dbSNP
12g.6021960C>TCA114160VWFc.3614G>A (p.Arg1205His)
ClinVar dbSNP

Number of alleles fetched