Canonical Allele Identifier: PA2827936096
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 950435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Tyr172Phe
CA389277925
NM_001354769.1:c.515A>T