Canonical Allele Identifier: PA356253
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 220554
ClinVar RCV Id: RCV000206504 RCV000575816 RCV001799634 RCV003468955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu179Val
CA350524
NM_002485.5:c.536A>T