Canonical Allele Identifier: PA2830189040
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2157196
ClinVar RCV Id: RCV003091108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579878.1:p.Gly29Ser
CA2811813
NM_133331.3:c.85G>A