Allele Registry

Canonical Allele Identifier: PA2825334418

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV001025091

RCV002551916

ClinVar Variation:

826300

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Val128Leu	CA371659210 NM_001024688.3:c.382G>C