ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829314617
Gene: CASP8
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2301833
ClinVar RCV Id:
RCV002886729
RCV003619814
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001387604.1:p.Cys22Arg
CA350294001
NM_001400675.1:c.64T>C