Canonical Allele Identifier: PA1139726587
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 848310
ClinVar RCV Id: RCV001052037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.His58Gln
CA393032045
NM_016346.4:c.174C>A
CA393032046
NM_016346.4:c.174C>G