Canonical Allele Identifier: PA2827491051
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 388568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336299.1:p.Arg1696Trp
CA16604601
NM_001349370.3:c.5086C>T