Canonical Allele Identifier: PA2825335524
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1463348
ClinVar RCV Id: RCV001997683 RCV002398019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Val498Gly
CA371655201
NM_001024688.3:c.1493T>G