Allele Registry

Canonical Allele Identifier: PA645465193

Gene: NBN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

240432

617505

ClinVar RCV:

RCV000228075

RCV000762529

RCV000772147

RCV000775704

RCV003475060

ClinVar Variation:

239195

630431

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Gly12Arg	CA10582607 NM_002485.5:c.34G>A CA371664132 NM_002485.5:c.34G>C