Canonical Allele Identifier: PA2827935947
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 937275
ClinVar RCV Id: RCV001206249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Cys176Tyr
CA389277785
NM_001354768.3:c.527G>A