Canonical Allele Identifier: PA2741897549
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2808777
ClinVar RCV Id: RCV003618360
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Lys288Glu
CA371658337
NM_002485.5:c.862A>G