Allele Registry

Canonical Allele Identifier: PA891856236

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000688246

RCV001176635

RCV001280672

RCV002485614

RCV003128640

ClinVar Variation:

568013

HGVS (amino-acid)	Matching Registered Transcripts
NP_002476.2:p.Gln326Glu	CA371656881 NM_002485.5:c.976C>G