Canonical Allele Identifier: PA235937
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 191061
ClinVar RCV Id: RCV000171238 RCV000787632 RCV001074909 RCV003468852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Gly216Ser
CA235935
NM_016346.4:c.646G>A