Canonical Allele Identifier: PA2829751288
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 999611
ClinVar RCV Id: RCV001295630 RCV001835392
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Ala102Ser
CA7640279
NM_014249.4:c.304G>T