Canonical Allele Identifier: PA2827263534
Gene: IFNGR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496111
ClinVar RCV Id: RCV001991719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316057.1:p.Pro3Arg
CA10006824
NM_001329128.2:c.8C>G