Canonical Allele Identifier: PA2825335641
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_001019859.1:p.Arg542Ser
CA371677270
NM_001024688.3:c.1624C>A