Allele Registry

Canonical Allele Identifier: PA916044694

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017529

ClinVar Variation:

16147

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351114.1:p.Asp642Val	CA126218 NM_001364185.1:c.1925A>T