Canonical Allele Identifier: PA915997043
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 801230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Thr516Ala
CA4802705
NM_002485.5:c.1546A>G