Canonical Allele Identifier: PA2741927098
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2865238
ClinVar RCV Id: RCV003697684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Glu55Gly
CA257868831
NM_006177.5:c.164A>G