Canonical Allele Identifier: PA2825401079
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202292
ClinVar RCV Id: RCV004493704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035889.1:p.Ser11Cys
CA2811801
NM_001042424.3:c.32C>G