Allele Registry

Canonical Allele Identifier: PA916044586

Gene: IRF8 HGNC NCBI

ClinVar RCV:

RCV000050230

ClinVar Variation:

56843

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350836.1:p.Thr90Ala	CA144516 NM_001363907.1:c.268A>G