Canonical Allele Identifier: PA2830189034
Gene: NSD2 HGNC NCBI
ClinVar RCV:
RCV004493704
ClinVar Variation:
3202292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579878.1:p.Ser11Cys
CA2811801
NM_133331.3:c.32C>G