Canonical Allele Identifier: PA2825335274
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1358453
ClinVar RCV Id: RCV001894221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Glu409Gly
CA371655784
NM_001024688.3:c.1226A>G