Canonical Allele Identifier: PA2825607574
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 517175
ClinVar RCV Id: RCV000611135 RCV000897752 RCV001160131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120925.1:p.Leu403Pro
CA4191357
NM_001127453.2:c.1208T>C