Allele Registry

Canonical Allele Identifier: PA2825335061

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000559800

RCV001010572

ClinVar Variation:

461497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Asn337His	CA4802771 NM_001024688.3:c.1009A>C