Canonical Allele Identifier: PA2825334447
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566725
ClinVar RCV Id: RCV003278162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Gln138Arg
CA371659080
NM_001024688.3:c.413A>G