Canonical Allele Identifier: PA2580409421
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2067732
ClinVar RCV Id: RCV002970608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Met89Val
CA7640274
NM_016346.4:c.265A>G