Allele Registry

Canonical Allele Identifier: PA2825334946

Gene: NBN HGNC NCBI

ClinVar Allele:

233661

ClinVar RCV:

RCV000218105

RCV001067296

ClinVar Variation:

229678

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ile302Met	CA10578769 NM_001024688.3:c.906C>G