Canonical Allele Identifier: PA645492987
Gene: NR3C2 HGNC NCBI

Linked Data

ClinVar Variation Id: 347725
ClinVar RCV Id: RCV000262756 RCV004021941
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Amino-acid Alleles

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