Allele Registry

Canonical Allele Identifier: PA2825335672

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000534847

ClinVar Variation:

461526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ala552Thr	CA371677210 NM_001024688.3:c.1654G>A