Canonical Allele Identifier: PA2741920579
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2918486
ClinVar RCV Id: RCV003615501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro1146Ser
CA393085317
NM_005477.3:c.3436C>T