Allele Registry

Canonical Allele Identifier: PA2828132235

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017529

ClinVar Variation:

16147

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351112.1:p.Asp642Val	CA126218 NM_001364183.2:c.1925A>T