Canonical Allele Identifier: PA645423767
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 348417
ClinVar RCV Id: RCV001309481 RCV004021960
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579877.1:p.Ser4Asn
CA2811799
NM_133330.3:c.11G>A