Canonical Allele Identifier: PA205876
Gene: NR0B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211685
ClinVar RCV Id: RCV000192799 RCV003977518
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068804.1:p.Asp178Asn
CA205875
NM_021969.3:c.532G>A