Canonical Allele Identifier: PA2580335745
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1947847
ClinVar RCV Id: RCV002663629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Met58Leu
CA257868829
NM_006177.5:c.172A>T
CA389281365
NM_006177.5:c.172A>C