Canonical Allele Identifier: PA339217
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 216565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asn520Ser
CA339215
NM_002485.5:c.1559A>G