Canonical Allele Identifier: PA2573226125
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1393089
ClinVar RCV Id: RCV001896553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ser204Pro
CA371659291
NM_002485.5:c.610T>C