Canonical Allele Identifier: PA2825335367
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1358634

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Thr442Ile
CA371655569
NM_001024688.3:c.1325C>T