Canonical Allele Identifier: PA2825335080
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 485920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Pro345Thr
CA371656207
NM_001024688.3:c.1033C>A