Allele Registry

Canonical Allele Identifier: PA299613

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000160786

RCV000212744

RCV001304232

ClinVar Variation:

182719

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Asn419Asp	CA299611 NM_002485.5:c.1255A>G