Canonical Allele Identifier: PA2827936107
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1297094
ClinVar RCV Id: RCV001724798 RCV002539736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Leu187Met
CA257868076
NM_001354769.1:c.559C>A