Canonical Allele Identifier: PA2827491190
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135204
ClinVar RCV Id: RCV000122016 RCV001719891 RCV004530034 RCV000652643 RCV002514650
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336299.1:p.Gly1923Asp
CA162005
NM_001349370.3:c.5768G>A