Allele Registry

Canonical Allele Identifier: PA299644

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000160798

RCV000197183

RCV000212724

RCV003467264

ClinVar Variation:

182731

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Pro6Ser	CA299642 NM_002485.5:c.16C>T