Canonical Allele Identifier: PA2827935868
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2865238
ClinVar RCV Id: RCV003697684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Glu55Gly
CA257868831
NM_001354768.3:c.164A>G