Canonical Allele Identifier: PA658816711
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 530765
ClinVar RCV Id: RCV000636780 RCV002404779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Lys579Gln
CA371655212
NM_002485.5:c.1735A>C