Allele Registry

Canonical Allele Identifier: PA916039340

Gene: NRL HGNC NCBI

ClinVar RCV:

RCV000015088

RCV003556022

ClinVar Variation:

14044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341699.1:p.Leu55Pro	CA123731 NM_001354770.2:c.164T>C