Canonical Allele Identifier: PA2741897691
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 2702798
ClinVar RCV Id: RCV003508020

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Pro498His
CA371655743
NM_002485.5:c.1493C>A