Canonical Allele Identifier: PA2827936072
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1429632
ClinVar RCV Id: RCV001939033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Ser139Trp
CA389278888
NM_001354769.1:c.416C>G