Allele Registry

Canonical Allele Identifier: PA162028

Gene: SETD2 HGNC NCBI

ClinVar RCV:

RCV000122023

RCV000652615

RCV001705897

RCV004542917

ClinVar Variation:

135211

HGVS (amino-acid)	Matching Registered Transcripts
NP_054878.5:p.Asn719Asp	CA162026 NM_014159.7:c.2155A>G