Canonical Allele Identifier: PA2825327636
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2719832
ClinVar RCV Id: RCV003553776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018085.1:p.Met86Val
CA3487105
NM_001018075.1:c.256A>G