Canonical Allele Identifier: PA2826760270
Gene: IFNAR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276054.1:p.Ile9Met
CA10005495
NM_001289125.3:c.27C>G