Canonical Allele Identifier: PA2825334632
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 185976
ClinVar RCV Id: RCV000165493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Ile200Thr
CA193540
NM_001024688.3:c.599T>C