Canonical Allele Identifier: PA2825334677
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 530719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asp213Val
CA371658217
NM_001024688.3:c.638A>T