Canonical Allele Identifier: PA2580229221
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2179792
ClinVar RCV Id: RCV002599322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Arg26Pro
CA389279088
NM_001354770.2:c.77G>C