Allele Registry

Canonical Allele Identifier: PA165952

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000130210

RCV000199051

RCV000499428

RCV000589088

RCV003474761

ClinVar Variation:

141617

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Asp577Tyr	CA165950 NM_002485.5:c.1729G>T