Canonical Allele Identifier: PA2580169668
Gene: HCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2216123
ClinVar RCV Id: RCV002691361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185.3:p.Gly748Arg
CA402887366
NM_001194.4:c.2242G>C
CA402887368
NM_001194.4:c.2242G>A