Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.94761900C>TCA10602359n.932-13158C>T (p.=)
ClinVar dbSNP gnomAD
10g.94761900C>ACA10576167n.932-13158C>A (p.=)
ClinVar dbSNP

Number of alleles fetched