Canonical Allele Identifier: PA2825334652
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_001019859.1:p.Lys206Glu
CA371658337
NM_001024688.3:c.616A>G