Canonical Allele Identifier: PA2825335398
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2089023
ClinVar RCV Id: RCV003011934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asn452Ser
CA371655506
NM_001024688.3:c.1355A>G