Canonical Allele Identifier: PA915981813
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 359850
ClinVar RCV Id: RCV000270022 RCV001375130 RCV001358026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120926.1:p.Asp40Val
CA4191671
NM_001127454.2:c.119A>T