Canonical Allele Identifier: PA2828131982
Gene: NR3C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2719832
ClinVar RCV Id: RCV003553776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351110.1:p.Met86Val
CA3487105
NM_001364181.2:c.256A>G