Canonical Allele Identifier: PA2825607758
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 359840
ClinVar RCV Id: RCV000291443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120926.1:p.His254Arg
CA10625875
NM_001127454.2:c.761A>G