Canonical Allele Identifier: PA658674368
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 452053
ClinVar RCV Id: RCV000523630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Trp461Arg
CA393094183
NM_005477.3:c.1381T>C
CA393094184
NM_005477.3:c.1381T>A