Canonical Allele Identifier: PA2580276962
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1986072
ClinVar RCV Id: RCV002785911 RCV004064730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Lys549Ile
CA371655409
NM_002485.5:c.1646A>T