Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.50523901G>ACA117676NCAPH2,SCO2c.511C>T (p.Arg171Trp)
c.*526G>A (n.*526G>A)
n.2554G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
22g.50523901G=CA2410905971NCAPH2,SCO2c.511C= (p.Arg171=)
c.*526G= (n.*526G=)
n.2554G=
dbSNP

Number of alleles fetched