Canonical Allele Identifier: PA117576
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 5532
ClinVar RCV Id: RCV000005869 RCV000005870 RCV000171240 RCV000393548 RCV000668086 RCV000787633 RCV001074891 RCV001095701 RCV001257807 RCV001374877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Arg311Gln
CA117575
NM_016346.4:c.932G>A