Canonical Allele Identifier: PA2830189381
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202300
ClinVar RCV Id: RCV004493712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579889.1:p.Lys17Asn
CA2811807
NM_133334.2:c.51G>C
CA355989151
NM_133334.2:c.51G>T