Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.122506802G>ACA340685HTRA1c.889G>A (p.Val297Met)
c.571G>A (p.Val191Met)
c.112G>A (p.Val38Met)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
10g.122506802G=CA1941477237HTRA1c.889G= (p.Val297=)
c.571G= (p.Val191=)
c.112G= (p.Val38=)
 dbSNP

Number of alleles fetched