Canonical Allele Identifier: PA2825334653
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 567651
ClinVar RCV Id: RCV000687801 RCV002369842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Trp207Gly
CA371658329
NM_001024688.3:c.619T>G