Canonical Allele Identifier: PA263241
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55874
ClinVar RCV Id: RCV000049288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Arg425Ile
CA263240
NM_000475.5:c.1274G>T