Canonical Allele Identifier: PA915956807
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 419295
ClinVar RCV Id: RCV000480445 RCV001276021
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001019859.1:p.Asp39Gly
CA4802991
NM_001024688.3:c.116A>G