Canonical Allele Identifier: PA2573081941
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 1313751
ClinVar RCV Id: RCV001769397 RCV003617938
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Glu559Lys
CA371655347
NM_002485.5:c.1675G>A