Allele Registry

Canonical Allele Identifier: PA658671942

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000536553

RCV000573249

ClinVar Variation:

461513

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Asn520Asp	CA181257926 NM_002485.5:c.1558A>G