Allele Registry

Canonical Allele Identifier: PA2825334997

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000167134

RCV000686355

ClinVar Variation:

187410

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Thr320Ala	CA197574 NM_001024688.3:c.958A>G