Canonical Allele Identifier: PA2825335357
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 216565
ClinVar RCV Id: RCV000200286 RCV000580918 RCV003324728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asn438Ser
CA339215
NM_001024688.3:c.1313A>G