Canonical Allele Identifier: PA2829751402
Gene: NR2E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 317013
ClinVar RCV Id: RCV000297664 RCV000369444 RCV001069768 RCV001119821 RCV003888733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055064.1:p.Ser137Phe
CA7640308
NM_014249.4:c.410C>T