Allele Registry

Canonical Allele Identifier: PA301959

Gene: HCN4 HGNC NCBI

ClinVar RCV:

RCV000170938

RCV000619663

RCV001051690

RCV002478538

ClinVar Variation:

190779

HGVS (amino-acid)	Matching Registered Transcripts
NP_005468.1:p.Arg378Cys	CA301958 NM_005477.3:c.1132C>T