Canonical Allele Identifier: PA2825335303
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1773865
ClinVar RCV Id: RCV002389782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Ser417Ile
CA2580079073
NM_001024688.3:c.1249_1250delinsAT