Canonical Allele Identifier: PA2827936022
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2794346
ClinVar RCV Id: RCV003672785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Gly57Asp
CA389281383
NM_001354769.1:c.170G>A