Canonical Allele Identifier: PA2829635559
Gene: NRL HGNC NCBI

Linked Data

ClinVar Variation Id: 1492711
ClinVar RCV Id: RCV001981169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006168.1:p.Met140Ile
CA389278865
NM_006177.5:c.420G>T
CA389278866
NM_006177.5:c.420G>C
CA389278867
NM_006177.5:c.420G>A