Canonical Allele Identifier: PA1139735121
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 937275
ClinVar RCV Id: RCV001206249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Cys71Tyr
CA389277785
NM_001354770.2:c.212G>A