Canonical Allele Identifier: PA2741867999
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 3001276
ClinVar RCV Id: RCV003852419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Leu23Pro
CA7122843
NM_001354770.2:c.68T>C