Canonical Allele Identifier: PA2827490197
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 542227
ClinVar RCV Id: RCV000652623 RCV001816638 RCV001719158 RCV004533417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336299.1:p.Lys585Glu
CA2363615
NM_001349370.3:c.1753A>G