Canonical Allele Identifier: PA2825607779
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 44841
ClinVar RCV Id: RCV000037972 RCV000330799 RCV000948760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120926.1:p.Phe281Tyr
CA135159
NM_001127454.2:c.842T>A