Canonical Allele Identifier: PA2825335317
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 840526
ClinVar RCV Id: RCV001042538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Glu423Lys
CA371655698
NM_001024688.3:c.1267G>A