Canonical Allele Identifier: PA2580132824
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1740615
ClinVar RCV Id: RCV002328266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Thr66Ile
CA371661650
NM_001024688.3:c.197C>T