Canonical Allele Identifier: PA2827935878
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1510220
ClinVar RCV Id: RCV002011601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Arg66Gly
CA7122912
NM_001354768.3:c.196C>G