Canonical Allele Identifier: PA2827490289
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336299.1:p.Asn675Asp
CA162026
NM_001349370.3:c.2023A>G