Canonical Allele Identifier: PA645466147
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 411787
ClinVar RCV Id: RCV000470877 RCV000563097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ala713Gly
CA16612646
NM_002485.5:c.2138C>G