Allele Registry

Canonical Allele Identifier: PA2825327695

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017535

ClinVar Variation:

16153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001018085.1:p.Val571Ala	CA126229 NM_001018075.1:c.1712T>C