Canonical Allele Identifier: PA2825335372
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 141971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asp443Glu
CA166976
NM_001024688.3:c.1329T>A
CA371655560
NM_001024688.3:c.1329T>G