Allele Registry

Canonical Allele Identifier: PA2825334433

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000007363

RCV000115802

RCV000121621

RCV000487932

RCV003891431

ClinVar Variation:

6948

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Arg133Trp	CA160990 NM_001024688.3:c.397C>T