Canonical Allele Identifier: PA2827936175
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1715886
ClinVar RCV Id: RCV002301584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Ser119Trp
CA389276245
NM_001354770.2:c.356C>G