Allele Registry

Canonical Allele Identifier: PA2826269317

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017529

ClinVar Variation:

16147

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191193.1:p.Asp306Val	CA126218 NM_001204264.2:c.917A>T