Canonical Allele Identifier: PA1139712664
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 840097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Arg1069Trp
CA7648870
NM_005477.3:c.3205C>T