Allele Registry

Canonical Allele Identifier: PA658807701

Gene: SETD2 HGNC NCBI

ClinVar RCV:

RCV000652617

ClinVar Variation:

542222

HGVS (amino-acid)	Matching Registered Transcripts
NP_054878.5:p.Lys941Arg	CA352525019 NM_014159.7:c.2822A>G