Canonical Allele Identifier: PA2580276976
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2125789
ClinVar RCV Id: RCV003043794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Lys568Glu
CA371655284
NM_002485.5:c.1702A>G