Canonical Allele Identifier: PA2826168931
Gene: HCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3104501
ClinVar RCV Id: RCV004399377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185.3:p.Ala735Thr
CA9018878
NM_001194.4:c.2203G>A