Allele Registry

Canonical Allele Identifier: PA2825335611

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000483770

RCV000551607

RCV000567792

RCV000985869

ClinVar Variation:

420214

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ile532Met	CA4802680 NM_001024688.3:c.1596A>G