Allele Registry

Canonical Allele Identifier: PA2580160145

Gene: NREP HGNC NCBI

ClinVar RCV:

RCV004240578

ClinVar Variation:

2401003

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135947.1:p.Arg12Gln	CA3366963 NM_001142475.2:c.35G>A