Allele Registry

Canonical Allele Identifier: PA2825334894

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000115777

RCV000217684

RCV000700024

RCV001818277

ClinVar Variation:

127855

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Val282Ala	CA287898 NM_001024688.3:c.845T>C