Canonical Allele Identifier: PA2827935938
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1513892
ClinVar RCV Id: RCV002026403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Arg165Pro
CA389278128
NM_001354768.3:c.494G>C