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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
Amyotrophic Lateral Sclerosis 1
USH2A c.8559-2A>G
Cystic Fibrosis
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Mutation Direct
Effortless mutation search and display tool
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Search criteria:
Gene:
HCN4
& Disease:
SND
, 1 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
191377
HCN4
c.3502_3505del
p.Phe1168fs (p.F1168fs)
NM_005477.3
M
MS
VUS
4
+
3
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