Canonical Allele Identifier: PA658665627
Gene: NR0B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 449569
ClinVar RCV Id: RCV000523542 RCV003419905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068804.1:p.Arg54Cys
CA709710
NM_021969.3:c.160C>T