Canonical Allele Identifier: PA2580117341
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1990828
ClinVar RCV Id: RCV002805872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Glu313Asp
CA10376335
NM_000475.5:c.939G>T
CA327975933
NM_000475.5:c.939G>C