Canonical Allele Identifier: PA915998015
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 650000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005468.1:p.Gly980Ala
CA7648918
NM_005477.3:c.2939G>C