Canonical Allele Identifier: PA162007
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135204
ClinVar RCV Id: RCV000122016 RCV001719891 RCV004530034 RCV000652643 RCV002514650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054878.5:p.Gly1967Asp
CA162005
NM_014159.7:c.5900G>A