Canonical Allele Identifier: PA2827935911
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2179792
ClinVar RCV Id: RCV002599322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Arg131Pro
CA389279088
NM_001354768.3:c.392G>C