Canonical Allele Identifier: PA182129
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 178334
ClinVar RCV Id: RCV000155078 RCV001568973
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004394.1:p.Gly373Asp
CA182128
NM_004403.3:c.1118G>A