Canonical Allele Identifier: PA167006
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 141979
ClinVar RCV Id: RCV000130735 RCV000543794 RCV001547889
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu658Gly
CA167004
NM_002485.5:c.1973A>G