Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.247424765C>TCA280958NLRP3c.1316C>T (p.Ala439Val)
c.1181C>T (p.Ala394Val)
c.1322C>T (p.Ala441Val)
n.1497C>T
ClinVar dbSNP gnomAD v4
1g.247424765C=CA1141581526NLRP3c.1316C= (p.Ala439=)
c.1181C= (p.Ala394=)
c.1322C= (p.Ala441=)
n.1497C=
dbSNP

Number of alleles fetched