Canonical Allele Identifier: PA2741897544
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2586813
ClinVar RCV Id: RCV003341872 RCV003477085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Pro266Arg
CA371658611
NM_002485.5:c.797C>G