Canonical Allele Identifier: PA2825334584
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1713724
ClinVar RCV Id: RCV002304299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Cys187Arg
CA371658588
NM_001024688.3:c.559T>C