Allele Registry

Canonical Allele Identifier: PA658672181

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000568915

RCV000704836

ClinVar Variation:

483985

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Ala710Pro	CA371675559 NM_002485.5:c.2128G>C