Canonical Allele Identifier: PA916044586
Gene: IRF8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56843
ClinVar RCV Id: RCV000050230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350836.1:p.Thr90Ala
CA144516
NM_001363907.1:c.268A>G