Allele Registry

Canonical Allele Identifier: PA658672081

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000534847

ClinVar Variation:

461526

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Ala634Thr	CA371677210 NM_002485.5:c.1900G>A