Allele Registry

Canonical Allele Identifier: PA2825334382

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000160780

RCV000205060

RCV000726896

RCV002229765

RCV003474833

ClinVar Variation:

182713

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Pro117Arg	CA299593 NM_001024688.3:c.350C>G