Allele Registry

Canonical Allele Identifier: PA2825334770

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000217834

RCV001853581

ClinVar Variation:

232149

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Gln244Arg	CA10578781 NM_001024688.3:c.731A>G