Allele Registry

Canonical Allele Identifier: PA2825335254

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000218203

RCV000473153

RCV001284189

RCV001800560

ClinVar Variation:

232337

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Thr403Met	CA4802717 NM_001024688.3:c.1208C>T