Canonical Allele Identifier: PA658674438
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 470665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Gly1097Arg
CA7648853
NM_005477.3:c.3289G>A
CA393085766
NM_005477.3:c.3289G>C