Canonical Allele Identifier: PA645510423
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 438229
ClinVar RCV Id: RCV000504973 RCV000809974 RCV001376214 RCV001449815 RCV001724033 RCV003464084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Ala256Glu
CA7640401
NM_016346.4:c.767C>A