Canonical Allele Identifier: PA2827935884
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 884209
ClinVar RCV Id: RCV001115180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Ala76Gly
CA389280814
NM_001354768.3:c.227C>G