Canonical Allele Identifier: PA2829635612
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1348715
ClinVar RCV Id: RCV002050903
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Gly186Arg
CA389277487
NM_006177.5:c.556G>A
CA389277494
NM_006177.5:c.556G>C