Allele Registry

Canonical Allele Identifier: PA658674902

Gene: IRF8 HGNC NCBI

ClinVar Allele:

467136

ClinVar RCV:

RCV000557109

RCV000656479

RCV001193620

RCV001200602

ClinVar Variation:

475393

HGVS (amino-acid)	Matching Registered Transcripts
NP_002154.1:p.Ala201Val	CA8217014 NM_002163.2:c.602C>T