Canonical Allele Identifier: PA2827935867
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1065724
ClinVar RCV Id: RCV001376379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Pro51His
CA389281582
NM_001354768.3:c.152C>A