Canonical Allele Identifier: PA658675522
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_714917.2:p.Ile263_Tyr265del
CA658657446
NM_153706.4:c.788_796del