Canonical Allele Identifier: PA2827935870
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1947847
ClinVar RCV Id: RCV002663629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Met58Leu
CA257868829
NM_001354768.3:c.172A>T
CA389281365
NM_001354768.3:c.172A>C