Canonical Allele Identifier: PA2580276596
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1763820
ClinVar RCV Id: RCV002414468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Cys285Phe
CA371658379
NM_002485.5:c.854G>T