Allele Registry

Canonical Allele Identifier: PA645459186

Gene: IRF8 HGNC NCBI

ClinVar Allele:

260131

ClinVar RCV:

RCV000255394

ClinVar Variation:

265520

HGVS (amino-acid)	Matching Registered Transcripts
NP_002154.1:p.Asp3Glu	CA10588628 NM_002163.2:c.9C>G CA397000072 NM_002163.2:c.9C>A