Allele Registry

Canonical Allele Identifier: PA2825334240

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV001178737

ClinVar Variation:

920158

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Arg7Gly	CA371662446 NM_001024688.3:c.19C>G