Canonical Allele Identifier: PA2829400160
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1424714
ClinVar RCV Id: RCV001923976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Val114Gly
CA371662123
NM_002485.5:c.341T>G