Canonical Allele Identifier: PA645510417
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 438227
ClinVar RCV Id: RCV000504667 RCV001074908 RCV001857226 RCV003464082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057430.1:p.Ala102Asp
CA7640280
NM_016346.4:c.305C>A