Canonical Allele Identifier: PA2825335635
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1374599
ClinVar RCV Id: RCV001900639 RCV004040626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Lys540Arg
CA371677282
NM_001024688.3:c.1619A>G