Allele Registry

Canonical Allele Identifier: PA2825335289

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000636740

RCV004025480

ClinVar Variation:

530739

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Pro413Ser	CA371655760 NM_001024688.3:c.1237C>T