Canonical Allele Identifier: PA658676785
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 475513
ClinVar RCV Id: RCV000548155 RCV001707740 RCV001821637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054878.5:p.His1162Tyr
CA2363373
NM_014159.7:c.3484C>T