Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.6018598A>TCA114119VWFc.4820T>A (p.Val1607Asp)
n.421-24664T>A
 ClinVar dbSNP
12g.6018598A=CA2013872590VWFc.4820T= (p.Val1607=)
n.421-24664T=
 dbSNP

Number of alleles fetched