Allele Registry

Canonical Allele Identifier: PA2826269337

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017538

ClinVar Variation:

16155

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191193.1:p.Leu438Pro	CA126234 NM_001204264.2:c.1313T>C