Allele Registry

Canonical Allele Identifier: PA2828127732

Gene: IRF8 HGNC NCBI

ClinVar RCV:

RCV000656480

RCV001242309

ClinVar Variation:

545494

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350837.1:p.Pro20Leu	CA8217026 NM_001363908.1:c.59C>T