Allele Registry

Canonical Allele Identifier: PA915956914

Gene: NBN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

233659

396309

ClinVar RCV:

RCV000217029

RCV000474157

RCV000486277

RCV000988085

RCV001797729

RCV001805080

RCV002478803

ClinVar Variation:

232551

411760

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ala318Thr	CA4802781 NM_001024688.3:c.952G>A CA16612365 NM_001024688.3:c.951_952delinsCA