Canonical Allele Identifier: PA2827936182
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1719071
ClinVar RCV Id: RCV002301831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Asp126Glu
CA389276086
NM_001354770.2:c.378C>G
CA389276088
NM_001354770.2:c.378C>A