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

Number of alleles fetched