Canonical Allele Identifier: PA2580276957
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2006891
ClinVar RCV Id: RCV002837974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Arg546Gly
CA371655434
NM_002485.5:c.1636A>G