Canonical Allele Identifier: PA2825335861
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 411748
ClinVar RCV Id: RCV000464532 RCV000562388 RCV001821291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Pro618Thr
CA16612356
NM_001024688.3:c.1852C>A