Canonical Allele Identifier: PA2830189033
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2662722
ClinVar RCV Id: RCV003441387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579878.1:p.Leu10Phe
CA355988898
NM_133331.3:c.28C>T