Canonical Allele Identifier: PA2827491082
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 222954
ClinVar RCV Id: RCV000208561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336299.1:p.Leu1771Trp
CA352148
NM_001349370.3:c.5312T>G