Canonical Allele Identifier: PA2827935863
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 966141
ClinVar RCV Id: RCV001240748 RCV003887951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Ser50Leu
CA389281613
NM_001354768.3:c.149C>T