Canonical Allele Identifier: PA2825334480
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2859532
ClinVar RCV Id: RCV003617560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Lys151Glu
CA371658929
NM_001024688.3:c.451A>G