Allele Registry

Canonical Allele Identifier: PA2825335413

Gene: NBN HGNC NCBI

ClinVar Allele:

233642

ClinVar RCV:

RCV000216784

RCV000460642

RCV003468996

ClinVar Variation:

230316

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ala459Gly	CA10578757 NM_001024688.3:c.1376C>G