Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.36288308T>CCA134546MYH9c.4939A>G (p.Ile1647Val)
n.5171A>G
c.4876A>G (p.Ile1626Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.36288308T=CA2403798190MYH9c.4939A= (p.Ile1647=)
n.5171A=
c.4876A= (p.Ile1626=)
 dbSNP

Number of alleles fetched