Canonical Allele Identifier: PA2499271229
Gene: IFNGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000970
ClinVar RCV Id: RCV001297183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005525.2:p.Ala21_Ala22del
CA748817333
NM_005534.4:c.57_62del