Allele Registry

Canonical Allele Identifier: PA645465855

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000217834

RCV001853581

ClinVar Variation:

232149

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Gln326Arg	CA10578781 NM_002485.5:c.977A>G