Allele Registry

Canonical Allele Identifier: PA916044595

Gene: IRF8 HGNC NCBI

ClinVar RCV:

RCV000656480

RCV001242309

ClinVar Variation:

545494

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350836.1:p.Pro234Leu	CA8217026 NM_001363907.1:c.701C>T