Canonical Allele Identifier: PA261138
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 39510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Met96Thr
CA261137
NM_006177.5:c.287T>C