Canonical Allele Identifier: PA2741897448
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566736
ClinVar RCV Id: RCV003306708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gln59Arg
CA371662637
NM_002485.5:c.176A>G