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disease: Deafness, autosomal dominant 20

id4896
nameDeafness, autosomal dominant 20
variant-disease NM_001614.5(ACTG1):c.994C>G (p.Pro332Ala) AND Deafness, autosomal dominant 20
NM_001614.5(ACTG1):c.791C>T (p.Pro264Leu) AND Deafness, autosomal dominant 20
NM_001614.5(ACTG1):c.833C>T (p.Thr278Ile) AND Deafness, autosomal dominant 20
NM_001614.5(ACTG1):c.353A>T (p.Lys118Met) AND Deafness, autosomal dominant 20
NM_001614.5(ACTG1):c.354G>C (p.Lys118Asn) AND Deafness, autosomal dominant 20
... 16 more