Canonical Allele Identifier: PA2825335487
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2125789
ClinVar RCV Id: RCV003043794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Lys486Glu
CA371655284
NM_001024688.3:c.1456A>G