Allele Registry

Canonical Allele Identifier: PA916044587

Gene: IRF8 HGNC NCBI

ClinVar RCV:

RCV000050229

ClinVar Variation:

56842

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350836.1:p.Lys118Glu	CA144514 NM_001363907.1:c.352A>G