Canonical Allele Identifier: PA2827936059
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 3028276
ClinVar RCV Id: RCV003889646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Gln124Pro
CA389279353
NM_001354769.1:c.371A>C