Canonical Allele Identifier: PA913192386
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 629040
ClinVar RCV Id: RCV001315586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Arg28Gly
CA371663424
NM_002485.5:c.82A>G