Canonical Allele Identifier: PA2825334443
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 530757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Lys137Arg
CA4802914
NM_001024688.3:c.410A>G