Canonical Allele Identifier: PA2741920443
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2964913
ClinVar RCV Id: RCV003828535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Ser831Phe
CA393088787
NM_005477.3:c.2492C>T