Canonical Allele Identifier: PA2829403926
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 3222428
ClinVar RCV Id: RCV004513842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Lys735Glu
CA371674802
NM_002485.5:c.2203A>G