Canonical Allele Identifier: PA645465679
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 418680
ClinVar RCV Id: RCV000481220 RCV000557130 RCV002323817 RCV004525942
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu111Gly
CA16618710
NM_002485.5:c.332A>G