Allele Registry

Canonical Allele Identifier: PA915995929

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV001025091

RCV002551916

ClinVar Variation:

826300

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Val210Leu	CA371659210 NM_002485.5:c.628G>C