Allele Registry

Canonical Allele Identifier: PA915956785

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000115793

ClinVar Variation:

127870

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Glu27Gln	CA287931 NM_001024688.3:c.79G>C