Canonical Allele Identifier: PA2580277011
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1714180
ClinVar RCV Id: RCV002297163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu625Ala
CA371677264
NM_002485.5:c.1874A>C