Canonical Allele Identifier: PA2830188701
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202292
ClinVar RCV Id: RCV004493704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579877.1:p.Ser11Cys
CA2811801
NM_133330.3:c.32C>G