Canonical Allele Identifier: PA2827935931
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 934886
ClinVar RCV Id: RCV001203366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Ala157Ser
CA389278412
NM_001354768.3:c.469G>T