Canonical Allele Identifier: PA2825335528
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 481842
ClinVar RCV Id: RCV000574278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Gln499Glu
CA371655200
NM_001024688.3:c.1495C>G