Canonical Allele Identifier: PA891851108
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 573242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro145Leu
CA7649475
NM_005477.3:c.434C>T