Allele Registry

Canonical Allele Identifier: PA645492987

Gene: NR3C2 HGNC NCBI

ClinVar RCV:

RCV000262756

RCV004021941

ClinVar Variation:

347725

HGVS (amino-acid)	Matching Registered Transcripts
NP_000892.2:p.Pro696Leu	CA3100176 NM_000901.5:c.2087C>T