Allele Registry

Canonical Allele Identifier: PA2827490317

Gene: SETD2 HGNC NCBI

ClinVar RCV:

RCV000652611

ClinVar Variation:

542219

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336299.1:p.Ser698Ala	CA2363567 NM_001349370.3:c.2092T>G