Allele Registry

Canonical Allele Identifier: PA2825335033

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000574288

RCV000694630

RCV000833202

ClinVar Variation:

480019

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ser329Cys	CA4802777 NM_001024688.3:c.986C>G