Canonical Allele Identifier: PA2825334661
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 134877
ClinVar RCV Id: RCV000121623 RCV000583974 RCV000666592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Gln209Arg
CA160996
NM_001024688.3:c.626A>G