Canonical Allele Identifier: PA333817
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 183076
ClinVar RCV Id: RCV000161942 RCV000574837 RCV002478492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Gly96Ser
CA333815
NM_002485.5:c.286G>A