Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47448072G>ACA5976769RAPSNc.271C>T (p.Arg91Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.47448072G>CCA380334784RAPSNc.271C>G (p.Arg91Gly)
dbSNP gnomAD v4
11g.47448072G=CA1969378552RAPSNc.271C= (p.Arg91=)
dbSNP

Number of alleles fetched