Canonical Allele Identifier: PA2827936069
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2875470
ClinVar RCV Id: RCV003707239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Val138Ala
CA389278896
NM_001354769.1:c.413T>C