Canonical Allele Identifier: PA658730174
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 490062
ClinVar RCV Id: RCV000581122 RCV001800799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Pro266Ala
CA4802885
NM_002485.5:c.796C>G