Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.50911804T>ACA341910PYGLc.1895A>T (p.Asn632Ile)
n.68A>T
c.1793A>T (p.Asn598Ile)
 ClinVar dbSNP gnomAD v4
14g.50911804T=CA2136416522PYGLc.1895A= (p.Asn632=)
n.68A=
c.1793A= (p.Asn598=)
 dbSNP

Number of alleles fetched