Allele Registry

Canonical Allele Identifier: PA2827935934

Gene: NRL HGNC NCBI

ClinVar RCV:

RCV000015088

RCV003556022

ClinVar Variation:

14044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341697.1:p.Leu160Pro	CA123731 NM_001354768.3:c.479T>C