Allele Registry

Canonical Allele Identifier: PA101148

Gene: NR3C1 HGNC NCBI

ClinVar RCV:

RCV000017529

ClinVar Variation:

16147

HGVS (amino-acid)	Matching Registered Transcripts
NP_000167.1:p.Asp641Val	CA126218 NM_000176.3:c.1922A>T