Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107791841T>ACA126853SLC26A3c.371A>T (p.His124Leu)
c.*162A>T (n.*162A>T)
ClinVar dbSNP gnomAD v4
7g.107791841T=CA1732797705SLC26A3c.371A= (p.His124=)
c.*162A= (n.*162A=)
dbSNP

Number of alleles fetched