Allele Registry

Canonical Allele Identifier: PA2825335315

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000566537

RCV000815889

ClinVar Variation:

481865

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Lys422Arg	CA4802708 NM_001024688.3:c.1265A>G