Canonical Allele Identifier: PA2829400148
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2120145
ClinVar RCV Id: RCV003059233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu111Gln
CA371662143
NM_002485.5:c.331G>C