Canonical Allele Identifier: PA2825607759
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 2657353
ClinVar RCV Id: RCV003436685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120926.1:p.Leu256Pro
CA4191308
NM_001127454.2:c.767T>C