Canonical Allele Identifier: PA236698
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 191450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Arg1154Gln
CA236697
NM_005477.3:c.3461G>A