Allele Registry

Canonical Allele Identifier: PA2825335784

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000160794

RCV000205938

RCV000235191

RCV001788054

RCV003317109

ClinVar Variation:

182727

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Asp595Asn	CA299630 NM_001024688.3:c.1783G>A