Allele Registry

Canonical Allele Identifier: PA1139726754

Gene: NR2E3 HGNC NCBI

ClinVar Variation Id: 867090

HGVS (amino-acid)	Matching Registered Transcripts
NP_057430.1:p.Arg97Cys	CA272574991 NM_016346.4:c.289C>T