Allele Registry

Canonical Allele Identifier: PA2825335463

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000216080

RCV000465308

ClinVar Variation:

231939

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ile476Val	CA10578755 NM_001024688.3:c.1426A>G