Canonical Allele Identifier: PA2829310609
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 642198
ClinVar RCV Id: RCV000795615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387577.1:p.Gly234Glu
CA350293942
NM_001400648.1:c.701G>A