Canonical Allele Identifier: PA2825335472
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 411742
ClinVar RCV Id: RCV000463767
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Val480Gly
CA16612535
NM_001024688.3:c.1439T>G