Allele Registry

Canonical Allele Identifier: PA916039467

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000395090

RCV003736740

ClinVar Variation:

347735

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341748.1:p.Arg247Trp	CA3100414 NM_001354819.1:c.739A>T