Canonical Allele Identifier: PA2830189376
Gene: NSD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 596675
ClinVar RCV Id: RCV000732584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_579889.1:p.Phe3Leu
CA355988690
NM_133334.2:c.7T>C
CA355988715
NM_133334.2:c.9T>A
CA355988719
NM_133334.2:c.9T>G