Canonical Allele Identifier: PA2499252073
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1297094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Leu82Met
CA257868076
NM_001354770.2:c.244C>A