Allele Registry

Canonical Allele Identifier: PA301967

Gene: HCN4 HGNC NCBI

ClinVar RCV:

RCV000223698

RCV000726145

RCV000989357

RCV002433736

ClinVar Variation:

190784

HGVS (amino-acid)	Matching Registered Transcripts
NP_005468.1:p.Ser935Phe	CA301966 NM_005477.3:c.2804C>T