Canonical Allele Identifier: PA915997596
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 660308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro165Ser
CA393097856
NM_005477.3:c.493C>T