Canonical Allele Identifier: PA2827938869
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3201950
ClinVar RCV Id: RCV004491295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Ser335Asn
CA358247701
NM_001354819.1:c.1004G>A