Product Details

SNP ID
rs28409415
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:594147 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGGCTGGGGCTGGAGGGGACACG[A/G]AGGCCCAGGGAGGGGCGGTCTGAGG
Phenotype
MIM: 602781
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HCN2 PubMed Links

Gene Details

Gene
HCN2
Gene Name
hyperpolarization activated cyclic nucleotide gated potassium channel 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001194.3 Intron NP_001185.3

View Full Product Details