Canonical Allele Identifier: PA2826018248
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8572
ClinVar RCV Id: RCV000009103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159576.1:p.Glu855Gly
CA119757
NM_001166104.2:c.2564A>G