Allele Registry

Canonical Allele Identifier: PA2825335060

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000160786

RCV000212744

RCV001304232

ClinVar Variation:

182719

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Asn337Asp	CA299611 NM_001024688.3:c.1009A>G