Canonical Allele Identifier: PA1139735116
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 950435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Tyr67Phe
CA389277925
NM_001354770.2:c.200A>T