Allele Registry

Canonical Allele Identifier: PA2827935861

Gene: NRL HGNC NCBI

ClinVar RCV:

RCV000015086

ClinVar Variation:

14042

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341697.1:p.Ser50Thr	CA257070 NM_001354768.3:c.148T>A