Allele Registry

Canonical Allele Identifier: PA645466069

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000471606

RCV000483350

RCV000569351

RCV001290536

RCV003476116

ClinVar Variation:

411782

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Ser615Pro	CA4802679 NM_002485.5:c.1843T>C