Canonical Allele Identifier: PA135170
Gene: GSDME HGNC NCBI

Linked Data

ClinVar Variation Id: 44847
ClinVar RCV Id: RCV000037978 RCV000329308 RCV002228130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004394.1:p.Val207Met
CA135169
NM_004403.3:c.619G>A