Allele Registry

Canonical Allele Identifier: PA2828132229

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017535

ClinVar Variation:

16153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351112.1:p.Val572Ala	CA126229 NM_001364183.2:c.1715T>C