Allele Registry

Canonical Allele Identifier: PA287933

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000115793

ClinVar Variation:

127870

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Glu109Gln	CA287931 NM_002485.5:c.325G>C