Allele Registry

Canonical Allele Identifier: PA2828132227

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017533

ClinVar Variation:

16151

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351112.1:p.Ile560Asn	CA126225 NM_001364183.2:c.1679T>A