Allele Registry

Canonical Allele Identifier: PA915995949

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV001025265

ClinVar Variation:

826403

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Arg215Gly	CA181276776 NM_002485.5:c.643C>G