Canonical Allele Identifier: PA2573225978
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1381437
ClinVar RCV Id: RCV001921957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Val26Ile
CA181281141
NM_002485.5:c.76G>A