Allele Registry

Canonical Allele Identifier: PA2828132039

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017533

ClinVar Variation:

16151

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351110.1:p.Ile559Asn	CA126225 NM_001364181.2:c.1676T>A