Canonical Allele Identifier: PA2573205712
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1492711
ClinVar RCV Id: RCV001981169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341699.1:p.Met35Ile
CA389278865
NM_001354770.2:c.105G>T
CA389278866
NM_001354770.2:c.105G>C
CA389278867
NM_001354770.2:c.105G>A