Canonical Allele Identifier: PA2825335971
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 550990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Glu655del
CA658822447
NM_001024688.3:c.1962_1964del