Canonical Allele Identifier: PA2825334637
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1763567
ClinVar RCV Id: RCV002447661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Pro201Leu
CA371658422
NM_001024688.3:c.602C>T