Canonical Allele Identifier: PA2827183895
Gene: SETD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 487781
ClinVar RCV Id: RCV000577837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309951.1:p.Ile111_Tyr113del
CA658657446
NM_001323022.1:c.332_340del