Allele Registry

Canonical Allele Identifier: PA197576

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000167134

RCV000686355

ClinVar Variation:

187410

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Thr402Ala	CA197574 NM_002485.5:c.1204A>G