Allele Registry

Canonical Allele Identifier: PA2828127575

Gene: IRF8 HGNC NCBI

ClinVar Allele:

260131

ClinVar RCV:

RCV000255394

ClinVar Variation:

265520

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350836.1:p.Asp13Glu	CA10588628 NM_001363907.1:c.39C>G CA397000072 NM_001363907.1:c.39C>A