Allele Registry

Canonical Allele Identifier: PA916044693

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017535

ClinVar Variation:

16153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351114.1:p.Val572Ala	CA126229 NM_001364185.1:c.1715T>C