Canonical Allele Identifier: PA913197686
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 595951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Leu795Phe
CA393088998
NM_005477.3:c.2383C>T