Canonical Allele Identifier: PA2741818202
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2928335
ClinVar RCV Id: RCV003787157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000466.2:p.Ala247Val
CA10376357
NM_000475.5:c.740C>T