Allele Registry

Canonical Allele Identifier: PA2825335888

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000568915

RCV000704836

ClinVar Variation:

483985

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ala628Pro	CA371675559 NM_001024688.3:c.1882G>C