Allele Registry

Canonical Allele Identifier: PA2825335039

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000222002

RCV000589729

RCV001087448

ClinVar Variation:

127857

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Asn331Ser	CA287901 NM_001024688.3:c.992A>G