Canonical Allele Identifier: PA2827183874
Gene: SETD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 487781
ClinVar RCV Id: RCV000577837
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001309947.1:p.Ile237_Tyr239del
CA658657446
NM_001323018.1:c.710_718del