Canonical Allele Identifier: PA915997206
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 819928
ClinVar RCV Id: RCV001012883
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp577Gly
CA371655222
NM_002485.5:c.1730A>G