Canonical Allele Identifier: PA162028
Gene: SETD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135211
ClinVar RCV Id: RCV000122023 RCV000652615 RCV004542917 RCV001705897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054878.5:p.Asn719Asp
CA162026
NM_014159.7:c.2155A>G