Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.5045742C>TCA6399898KCNA5c.1595C>T (p.Pro532Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.5045742C>ACA383466827KCNA5c.1595C>A (p.Pro532Gln)
dbSNP
12g.5045742C=CA2013431366KCNA5c.1595C= (p.Pro532=)
dbSNP

Number of alleles fetched