Canonical Allele Identifier: PA1139712641
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 935983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Pro1034Ser
CA393086215
NM_005477.3:c.3100C>T