Allele Registry

Canonical Allele Identifier: PA2825334437

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000688542

RCV001025298

ClinVar Variation:

568245

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Gln134Lys	CA181276755 NM_001024688.3:c.400C>A