Canonical Allele Identifier: PA2825335362
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2091959
ClinVar RCV Id: RCV002991753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Leu440del
CA2580079066
NM_001024688.3:c.1320_1322del