Allele Registry

Canonical Allele Identifier: PA108028

Gene: NRL HGNC NCBI

ClinVar RCV:

RCV000015086

ClinVar Variation:

14042

HGVS (amino-acid)	Matching Registered Transcripts
NP_006168.1:p.Ser50Thr	CA257070 NM_006177.5:c.148T>A