Allele Registry

Canonical Allele Identifier: PA915956826

Gene: NBN HGNC NCBI

ClinVar Allele:

396988

ClinVar RCV:

RCV000460586

RCV001021549

RCV001800688

ClinVar Variation:

411750

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ile50Met	CA16612674 NM_001024688.3:c.150A>G