Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.36289096C>TCA411379606MYH9c.4609G>A (p.Val1537Met)
n.4841G>A
c.4546G>A (p.Val1516Met)
 ClinVar dbSNP gnomAD v4
22g.36289096C>ACA273196MYH9c.4609G>T (p.Val1537Leu)
n.4841G>T
c.4546G>T (p.Val1516Leu)
 ClinVar dbSNP

Number of alleles fetched