Canonical Allele Identifier: PA645376159
Gene: HCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423436
ClinVar RCV Id: RCV000478576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001185.3:p.Pro543Leu
CA16620908
NM_001194.4:c.1628C>T