Canonical Allele Identifier: PA301965
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 190783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Ala843Thr
CA301964
NM_005477.3:c.2527G>A