Canonical Allele Identifier: PA163610
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 140805
ClinVar Variation Id: 1752959
ClinVar RCV Id: RCV002354042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp211Glu
CA163608
NM_002485.5:c.633T>A
CA371659184
NM_002485.5:c.633T>G