Canonical Allele Identifier: PA287924
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 127866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asn731Tyr
CA287922
NM_002485.5:c.2191A>T