Allele Registry

Canonical Allele Identifier: PA2825335276

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000213507

RCV000559007

RCV000732065

ClinVar Variation:

230440

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Gln410Lys	CA10578762 NM_001024688.3:c.1228C>A