Canonical Allele Identifier: PA658807724
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 521888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054878.5:p.Ala1124Val
CA2363394
NM_014159.7:c.3371C>T