Allele Registry

Canonical Allele Identifier: PA891856167

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000688542

RCV001025298

ClinVar Variation:

568245

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Gln216Lys	CA181276755 NM_002485.5:c.646C>A