Allele Registry

Canonical Allele Identifier: PA287936

Gene: NBN HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

133329

2062852

ClinVar RCV:

RCV000115795

RCV000197783

RCV000509203

RCV000515395

RCV000781635

RCV001356300

RCV002816679

RCV003467061

ClinVar Variation:

127872

2008778

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Met152Ile	CA287934 NM_002485.5:c.456G>A CA371661585 NM_002485.5:c.456G>T CA371661588 NM_002485.5:c.456G>C