Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142113T>CCA020207VHLc.266T>C (p.Leu89Pro)
 ClinVar dbSNP
3g.10142113T>ACA16602514VHLc.266T>A (p.Leu89His)
 ClinVar dbSNP COSMIC

Number of alleles fetched