Canonical Allele Identifier: PA2827935871
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2275055
ClinVar RCV Id: RCV002817695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Met58Thr
CA389281344
NM_001354768.3:c.173T>C