Canonical Allele Identifier: PA915997673
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 660645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Arg390Cys
CA272684408
NM_005477.3:c.1168C>T