Canonical Allele Identifier: PA166518
Gene: NBN HGNC NCBI

Linked Data

ClinVar Variation Id: 141816
ClinVar RCV Id: RCV000130482 RCV000486308 RCV000459979 RCV001193649 RCV003474763
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002476.2:p.Asp95Gly
CA166516
NM_002485.5:c.284A>G