Canonical Allele Identifier: PA301972
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 190787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro174Ser
CA301971
NM_005477.3:c.520C>T