Canonical Allele Identifier: PA658671926
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 461510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ser509Tyr
CA371655668
NM_002485.5:c.1526C>A