Allele Registry

Canonical Allele Identifier: PA2825334863

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000484152

RCV000527248

RCV001009794

ClinVar Variation:

418976

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ser273Gly	CA4802810 NM_001024688.3:c.817A>G