Canonical Allele Identifier: PA645466121
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 230295
ClinVar RCV Id: RCV000213231 RCV001828089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Arg670Gly
CA10578747
NM_002485.5:c.2008A>G