Canonical Allele Identifier: PA2825607585
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 2657353
ClinVar RCV Id: RCV003436685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120925.1:p.Leu420Pro
CA4191308
NM_001127453.2:c.1259T>C