Canonical Allele Identifier: PA658807701
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 542222
ClinVar RCV Id: RCV000652617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054878.5:p.Lys941Arg
CA352525019
NM_014159.7:c.2822A>G