Canonical Allele Identifier: PA2829635605
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 937275
ClinVar RCV Id: RCV001206249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Cys176Tyr
CA389277785
NM_006177.5:c.527G>A