Canonical Allele Identifier: PA915995501
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 662531
ClinVar RCV Id: RCV000820194 RCV002408973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Val26Ala
CA4803059
NM_002485.5:c.77T>C