Canonical Allele Identifier: PA645465839
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 421530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Met294Thr
CA4802879
NM_002485.5:c.881T>C