Canonical Allele Identifier: PA645465202
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 230415
ClinVar RCV Id: RCV000218564 RCV001363922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Cys31Arg
CA10578815
NM_002485.5:c.91T>C