Canonical Allele Identifier: PA2825334419
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 826323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asp129His
CA371659194
NM_001024688.3:c.385G>C