Canonical Allele Identifier: PA2829312387
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721167
ClinVar RCV Id: RCV002294857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387589.1:p.Arg218Gly
CA350293892
NM_001400660.1:c.652C>G