Allele Registry

Canonical Allele Identifier: PA189937

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000164059

RCV000473711

RCV000483231

RCV001354099

ClinVar Variation:

184749

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Arg89Pro	CA189935 NM_002485.5:c.266G>C