Canonical Allele Identifier: PA658816674
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 530737
ClinVar RCV Id: RCV000636735
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.His507Tyr
CA371655681
NM_002485.5:c.1519C>T