Allele Registry

Canonical Allele Identifier: PA916044594

Gene: IRF8 HGNC NCBI

ClinVar Allele:

467136

ClinVar RCV:

RCV000557109

RCV000656479

RCV001193620

RCV001200602

ClinVar Variation:

475393

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350836.1:p.Ala211Val	CA8217014 NM_001363907.1:c.632C>T