Canonical Allele Identifier: PA2825335532
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2566740
ClinVar RCV Id: RCV003278169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Glu502Gln
CA371655177
NM_001024688.3:c.1504G>C