Canonical Allele Identifier: PA2827936030
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1510220
ClinVar RCV Id: RCV002011601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Arg66Gly
CA7122912
NM_001354769.1:c.196C>G