Canonical Allele Identifier: PA915996177
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 656448
ClinVar RCV Id: RCV000812872 RCV002257980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gln279Glu
CA371658491
NM_002485.5:c.835C>G