Allele Registry

Canonical Allele Identifier: PA916060781

Gene: NSD2 HGNC NCBI

ClinVar Variation Id: 596675

HGVS (amino-acid)	Matching Registered Transcripts
NP_579890.1:p.Phe3Leu	CA355988690 NM_133335.4:c.7T>C CA355988715 NM_133335.4:c.9T>A CA355988719 NM_133335.4:c.9T>G