Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142139T>CCA020246VHLc.292T>C (p.Tyr98His)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.10142139T>ACA351750883VHLc.292T>A (p.Tyr98Asn)
 ClinVar dbSNP COSMIC

Number of alleles fetched