Allele Registry

Canonical Allele Identifier: PA2825335905

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000575176

RCV000636782

RCV001584370

ClinVar Variation:

480065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Arg632Gly	CA4802601 NM_001024688.3:c.1894C>G