Canonical Allele Identifier: PA2827935893
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 39510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Met96Thr
CA261137
NM_001354768.3:c.287T>C