Canonical Allele Identifier: PA2580276921
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2091959
ClinVar RCV Id: RCV002991753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Leu522del
CA2580079066
NM_002485.5:c.1566_1568del