Canonical Allele Identifier: PA658828802
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 550990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu737del
CA658822447
NM_002485.5:c.2208_2210del