Allele Registry

Canonical Allele Identifier: PA658671784

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000572328

RCV001041861

ClinVar Variation:

483975

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Lys423Arg	CA371656233 NM_002485.5:c.1268A>G