Canonical Allele Identifier: PA1139726745
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 987298
ClinVar RCV Id: RCV001268624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Gly88Val
CA393032364
NM_016346.4:c.263G>T