Allele Registry

Canonical Allele Identifier: PA915956896

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000576061

RCV000636728

ClinVar Variation:

480020

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ile89Leu	CA181279296 NM_001024688.3:c.265A>C