Allele Registry

Canonical Allele Identifier: PA2827490588

Gene: SETD2 HGNC NCBI

ClinVar RCV:

RCV000122047

RCV001518643

RCV001610430

ClinVar Variation:

135235

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336299.1:p.Met1036Ile	CA162098 NM_001349370.3:c.3108G>A CA352523233 NM_001349370.3:c.3108G>T CA352523235 NM_001349370.3:c.3108G>C