Canonical Allele Identifier: PA913192632
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 632918
ClinVar RCV Id: RCV000780525 RCV002397557 RCV001873187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ser535Ala
CA371655500
NM_002485.5:c.1603T>G