Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.209633102C>GCA257285LAMB3c.596G>C (p.Gly199Ala)
c.404G>C (p.Gly135Ala)
 ClinVar dbSNP gnomAD v4
1g.209633102C=CA1141581388LAMB3c.596G= (p.Gly199=)
c.404G= (p.Gly135=)
 dbSNP

Number of alleles fetched