Canonical Allele Identifier: PA2827936070
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1508063
ClinVar RCV Id: RCV002040321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341698.1:p.Val138Leu
CA389278923
NM_001354769.1:c.412G>C