Canonical Allele Identifier: PA112443
Gene: NR0B1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Trp291Cys
CA255634
NM_000475.5:c.873G>C
CA412547486
NM_000475.5:c.873G>T