Allele Registry

Canonical Allele Identifier: PA658671780

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000559800

RCV001010572

ClinVar Variation:

461497

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Asn419His	CA4802771 NM_002485.5:c.1255A>C