Canonical Allele Identifier: PA193542
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 185976
ClinVar RCV Id: RCV000165493
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Ile282Thr
CA193540
NM_002485.5:c.845T>C