Allele Registry

Canonical Allele Identifier: PA2827938918

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000009103

ClinVar Variation:

8572

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341748.1:p.Glu855Gly	CA119757 NM_001354819.1:c.2564A>G