Canonical Allele Identifier: PA2825335328
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 461510
ClinVar RCV Id: RCV000535492 RCV000566294
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Ser427Tyr
CA371655668
NM_001024688.3:c.1280C>A