Canonical Allele Identifier: PA891851165
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 570401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Ala840Thr
CA7649009
NM_005477.3:c.2518G>A