Canonical Allele Identifier: PA891856212
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 576339
ClinVar RCV Id: RCV000698817

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Cys285Gly
CA371658388
NM_002485.5:c.853T>G