Canonical Allele Identifier: PA2499252088
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045907
ClinVar RCV Id: RCV001350390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341748.1:p.Val395Phe
CA358247162
NM_001354819.1:c.1183G>T