Allele Registry

Canonical Allele Identifier: PA2825335265

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000164141

RCV000197233

RCV001354892

RCV003467286

ClinVar Variation:

184816

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Leu407Val	CA190135 NM_001024688.3:c.1219C>G