Canonical Allele Identifier: PA355311
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 220473
ClinVar RCV Id: RCV000204340 RCV003477699 RCV004020532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ala265Val
CA348590
NM_002485.5:c.794C>T