Canonical Allele Identifier: PA2580169664
Gene: HCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2385939
ClinVar RCV Id: RCV002689758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185.3:p.Pro721Leu
CA9018860
NM_001194.4:c.2162C>T