Allele Registry

Canonical Allele Identifier: PA2825335736

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000195616

RCV000486313

RCV000566063

RCV001731429

RCV003407708

ClinVar Variation:

216567

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Arg578Thr	CA335799 NM_001024688.3:c.1733G>C