Canonical Allele Identifier: PA2580117362
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2184211
ClinVar RCV Id: RCV002615735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Ala347Glu
CA10376316
NM_000475.5:c.1040C>A