Canonical Allele Identifier: PA2580330429
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1798435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Glu995Asp
CA393086573
NM_005477.3:c.2985G>T
CA393086575
NM_005477.3:c.2985G>C