Canonical Allele Identifier: PA163179
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 137542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro883Arg
CA163178
NM_005477.3:c.2648C>G