Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.36288285C>ACA514352342MYH9c.4962G>T (p.Arg1654=)
n.5194G>T
c.4899G>T (p.Arg1633=)
 dbSNP
22g.36288285C>TCA134549MYH9c.4962G>A (p.Arg1654=)
n.5194G>A
c.4899G>A (p.Arg1633=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched