Canonical Allele Identifier: PA162052
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135219
ClinVar RCV Id: RCV000122031 RCV000547348 RCV003436936 RCV004530037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054878.5:p.Thr592Lys
CA162050
NM_014159.7:c.1775C>A