Canonical Allele Identifier: PA2829751101
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2133877
ClinVar RCV Id: RCV003044660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Ser53Gly
CA393032007
NM_014249.4:c.157A>G