Canonical Allele Identifier: PA2827935874
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 2797511
ClinVar RCV Id: RCV003673250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341697.1:p.Val59Leu
CA389281296
NM_001354768.3:c.175G>T
CA389281310
NM_001354768.3:c.175G>C