Canonical Allele Identifier: PA2830189050
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2535770
ClinVar RCV Id: RCV003261209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579878.1:p.Ala70Asp
CA2811836
NM_133331.3:c.209C>A