Canonical Allele Identifier: PA2827935920
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1906500
ClinVar RCV Id: RCV002586960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Met140Leu
CA389278874
NM_001354768.3:c.418A>T
CA389278881
NM_001354768.3:c.418A>C