Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.88726546C>TCA352204PIEZO1c.3796+1G>A (n.3796+1G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.88726546C>GCA397102669PIEZO1c.3796+1G>C (n.3796+1G>C)
dbSNP gnomAD v2 gnomAD v4
16g.88726546C=CA2241253598PIEZO1c.3796+1G= (n.3796+1G=)
dbSNP

Number of alleles fetched