Canonical Allele Identifier: PA2573081927
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1332498
ClinVar RCV Id: RCV001805544 RCV002542406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asn666Thr
CA371676470
NM_002485.5:c.1997A>C