Canonical Allele Identifier: PA2825334615
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 230459
ClinVar RCV Id: RCV000221665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asn195Ser
CA10578790
NM_001024688.3:c.584A>G