Canonical Allele Identifier: PA2825335992
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1370386
ClinVar RCV Id: RCV001877138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Leu661Ile
CA181268717
NM_001024688.3:c.1981C>A