Allele Registry

Canonical Allele Identifier: PA160980

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000115794

RCV000121617

RCV000168260

RCV000515292

RCV000589414

RCV001355243

RCV003492491

ClinVar Variation:

127871

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Asn142Ser	CA160978 NM_002485.5:c.425A>G