Allele Registry

Canonical Allele Identifier: PA2825335596

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000166446

RCV000586042

RCV000636773

ClinVar Variation:

186796

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Glu524Lys	CA195896 NM_001024688.3:c.1570G>A