Canonical Allele Identifier: PA2825334676
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1764847
ClinVar RCV Id: RCV002373801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asp213Asn
CA181276279
NM_001024688.3:c.637G>A