Canonical Allele Identifier: PA2830189042
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2633986
ClinVar RCV Id: RCV003400428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579878.1:p.Ser30Gly
CA355989587
NM_133331.3:c.88A>G