Allele Registry

Canonical Allele Identifier: PA658827816

Gene: IRF8 HGNC NCBI

ClinVar RCV:

RCV000656480

RCV001242309

ClinVar Variation:

545494

HGVS (amino-acid)	Matching Registered Transcripts
NP_002154.1:p.Pro224Leu	CA8217026 NM_002163.2:c.671C>T