Allele Registry

Canonical Allele Identifier: PA645498946

Gene: HCN4 HGNC NCBI

ClinVar RCV:

RCV000415571

ClinVar Variation:

374861

HGVS (amino-acid)	Matching Registered Transcripts
NP_005468.1:p.Ala414Gly	CA16043944 NM_005477.3:c.1241C>G