Canonical Allele Identifier: PA658816691
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 530766
ClinVar RCV Id: RCV000636781 RCV000780527 RCV001292842 RCV002404780
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Val556Met
CA4802691
NM_002485.5:c.1666G>A