Canonical Allele Identifier: PA1139708081
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 919575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu736Gln
CA371674795
NM_002485.5:c.2206G>C