Canonical Allele Identifier: PA658731360
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 3222411
ClinVar RCV Id: RCV004513825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp525Gly
CA371655562
NM_002485.5:c.1574A>G