Allele Registry

Canonical Allele Identifier: PA916027687

Gene: IFNGR2 HGNC NCBI

ClinVar RCV:

RCV000015848

ClinVar Variation:

14727

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316057.1:p.Thr187Asn	CA124287 NM_001329128.2:c.560C>A