Canonical Allele Identifier: PA915996243
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 822686
ClinVar RCV Id: RCV001018239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gln291Pro
CA371658284
NM_002485.5:c.872A>C