Canonical Allele Identifier: PA2741897738
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2854950
ClinVar RCV Id: RCV003617497 RCV004371843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Arg624Ser
CA371677270
NM_002485.5:c.1870C>A