Canonical Allele Identifier: PA2830189038
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304199
ClinVar RCV Id: RCV001751966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579878.1:p.Ile27Ser
CA355989460
NM_133331.3:c.80T>G