Allele Registry

Canonical Allele Identifier: PA2825335390

Gene: NBN HGNC NCBI

ClinVar Allele:

151956

ClinVar RCV:

RCV000131247

RCV000542468

RCV001357760

RCV001778752

ClinVar Variation:

142242

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Ile449Val	CA167864 NM_001024688.3:c.1345A>G