Canonical Allele Identifier: PA2827936063
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 3001276
ClinVar RCV Id: RCV003852419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Leu128Pro
CA7122843
NM_001354769.1:c.383T>C