Canonical Allele Identifier: PA2825335324
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 948266
ClinVar RCV Id: RCV001219487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.His425Pro
CA371655680
NM_001024688.3:c.1274A>C