Canonical Allele Identifier: PA2826760476
Gene: IFNAR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444810
ClinVar RCV Id: RCV001982607 RCV004043698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276055.1:p.Ile9Met
CA10005495
NM_001289126.2:c.27C>G