Canonical Allele Identifier: PA2741839579
Gene: HCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2595033
ClinVar RCV Id: RCV003351181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185.3:p.Gln722Pro
CA9018861
NM_001194.4:c.2165A>C