Allele Registry

Canonical Allele Identifier: PA2826268918

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017533

ClinVar Variation:

16151

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191187.1:p.Ile533Asn	CA126225 NM_001204258.1:c.1598T>A