Allele Registry

Canonical Allele Identifier: PA103162

Gene: IRF8 HGNC NCBI

ClinVar RCV:

RCV000050230

ClinVar Variation:

56843

HGVS (amino-acid)	Matching Registered Transcripts
NP_002154.1:p.Thr80Ala	CA144516 NM_002163.2:c.238A>G