Allele Registry

Canonical Allele Identifier: PA2825334265

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000160793

RCV000636730

RCV002433715

ClinVar Variation:

182726

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ile15Val	CA299627 NM_001024688.3:c.43A>G