Allele Registry

Canonical Allele Identifier: PA2825334435

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV001025265

ClinVar Variation:

826403

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Arg133Gly	CA181276776 NM_001024688.3:c.397C>G