Allele Registry

Canonical Allele Identifier: PA645465205

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000217641

RCV000469351

ClinVar Variation:

230140

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Asn37Asp	CA10578814 NM_002485.5:c.109A>G