Canonical Allele Identifier: PA2825334673
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 421530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Met212Thr
CA4802879
NM_001024688.3:c.635T>C