Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.74259621G>CCA124413VSX2c.599G>C (p.Arg200Pro)
n.599G>C (p.Arg200Pro)
ClinVar dbSNP
14g.74259621G>ACA124412VSX2c.599G>A (p.Arg200Gln)
n.599G>A (p.Arg200Gln)
ClinVar dbSNP gnomAD

Number of alleles fetched