Canonical Allele Identifier: PA174423
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 161598
ClinVar RCV Id: RCV000149134 RCV000667547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Lys82Glu
CA174421
NM_002485.5:c.244A>G