Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142116A>CCA351750709VHLc.269A>C (p.Asn90Thr)
 ClinVar dbSNP
3g.10142116A>GCA020212VHLc.269A>G (p.Asn90Ser)
 ClinVar dbSNP gnomAD v4
3g.10142116A>TCA357043VHLc.269A>T (p.Asn90Ile)
 ClinVar dbSNP COSMIC

Number of alleles fetched