rs754764304

This variant is located in the HCN1 gene.

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ClinVar annotation

Likely Benign★★★☆
2 submitters1 publication

Inborn genetic diseases; Developmental and epileptic encephalopathy

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About HCN1

The membrane protein encoded by this gene is a hyperpolarization-activated cation channel that contributes to the native pacemaker currents in heart and neurons. The encoded protein can homodimerize or heterodimerize with other pore-forming subunits to form a potassium channel. This channel may act as a receptor for sour tastes. [provided by RefSeq, Oct 2011]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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