ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827490289
Gene: SETD2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000122023
RCV000652615
RCV001705897
RCV004542917
ClinVar Variation:
135211
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001336299.1:p.Asn675Asp
CA162026
NM_001349370.3:c.2023A>G