Allele Registry

Canonical Allele Identifier: PA199639

Gene: IRF7 HGNC NCBI

ClinVar RCV:

RCV000170460

ClinVar Variation:

190237

HGVS (amino-acid)	Matching Registered Transcripts
NP_001563.2:p.Phe410Val	CA199638 NM_001572.5:c.1228T>G