Canonical Allele Identifier: PA645498932
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 412784

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Asp364Asn
CA7649370
NM_005477.3:c.1090G>A